Canonical Allele Identifier: CA1260145445
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71655831A= , CM000664.2:g.71655831A= GRCh38
NC_000002.11:g.71882961A= , CM000664.1:g.71882961A= GRCh37
NC_000002.10:g.71736469A= NCBI36
NG_008694.1:g.207209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.2041-331A= ENSP00000513536.1:n.2041-331A=
ENST00000698058.1:c.1258-331A= ENSP00000513537.1:n.1258-331A=
ENST00000698059.1:c.1366-331A= ENSP00000513538.1:n.1366-331A=
ENST00000258104.8:c.4510-331A= MANE Plus Clinical ENSP00000258104.3:n.4510-331A=
ENST00000410020.8:c.4627-331A= MANE Select ENSP00000386881.3:n.4627-331A=
ENST00000258104.7:c.4510-331A= ENSP00000258104.3:n.4510-331A=
ENST00000394120.6:c.4513-331A= ENSP00000377678.2:n.4513-331A=
ENST00000409366.5:c.4576-331A= ENSP00000386512.1:n.4576-331A=
ENST00000409582.7:c.4624-331A= ENSP00000386547.3:n.4624-331A=
ENST00000409651.5:c.4606-331A= ENSP00000386683.1:n.4606-331A=
ENST00000409744.5:c.4534-331A= ENSP00000386285.1:n.4534-331A=
ENST00000409762.5:c.4561-331A= ENSP00000387137.1:n.4561-331A=
ENST00000410020.7:c.4627-331A= ENSP00000386881.3:n.4627-331A=
ENST00000410041.1:c.4564-331A= ENSP00000386617.1:n.4564-331A=
ENST00000413539.6:c.4603-331A= ENSP00000407046.2:n.4603-331A=
ENST00000429174.6:c.4573-331A= ENSP00000398305.2:n.4573-331A=
ENST00000479049.6:n.1395-331A=
NM_001130455.1:c.4513-331A= NP_001123927.1:n.4513-331A=
NM_001130976.1:c.4468-331A= NP_001124448.1:n.4468-331A=
NM_001130977.1:c.4531-331A= NP_001124449.1:n.4531-331A=
NM_001130978.1:c.4573-331A= NP_001124450.1:n.4573-331A=
NM_001130979.1:c.4603-331A= NP_001124451.1:n.4603-331A=
NM_001130980.1:c.4561-331A= NP_001124452.1:n.4561-331A=
NM_001130981.1:c.4624-331A= NP_001124453.1:n.4624-331A=
NM_001130982.1:c.4606-331A= NP_001124454.1:n.4606-331A=
NM_001130983.1:c.4576-331A= NP_001124455.1:n.4576-331A=
NM_001130984.1:c.4534-331A= NP_001124456.1:n.4534-331A=
NM_001130985.1:c.4564-331A= NP_001124457.1:n.4564-331A=
NM_001130986.1:c.4471-331A= NP_001124458.1:n.4471-331A=
NM_001130987.1:c.4627-331A= NP_001124459.1:n.4627-331A=
NM_003494.3:c.4510-331A= NP_003485.1:n.4510-331A=
XM_005264584.3:c.4669-331A= XP_005264641.1:n.4669-331A=
XM_005264585.3:c.4666-331A= XP_005264642.1:n.4666-331A=
XM_005264584.4:c.4669-331A= XP_005264641.1:n.4669-331A=
XM_005264585.5:c.4666-331A= XP_005264642.1:n.4666-331A=
XR_001738969.1:n.4827-331A=
NM_001130987.2:c.4627-331A= MANE Select NP_001124459.1:n.4627-331A=
NM_001130455.2:c.4513-331A= NP_001123927.1:n.4513-331A=
NM_001130976.2:c.4468-331A= NP_001124448.1:n.4468-331A=
NM_001130977.2:c.4531-331A= NP_001124449.1:n.4531-331A=
NM_001130978.2:c.4573-331A= NP_001124450.1:n.4573-331A=
NM_001130979.2:c.4603-331A= NP_001124451.1:n.4603-331A=
NM_001130980.2:c.4561-331A= NP_001124452.1:n.4561-331A=
NM_001130981.2:c.4624-331A= NP_001124453.1:n.4624-331A=
NM_001130982.2:c.4606-331A= NP_001124454.1:n.4606-331A=
NM_001130983.2:c.4576-331A= NP_001124455.1:n.4576-331A=
NM_001130984.2:c.4534-331A= NP_001124456.1:n.4534-331A=
NM_001130985.2:c.4564-331A= NP_001124457.1:n.4564-331A=
NM_001130986.2:c.4471-331A= NP_001124458.1:n.4471-331A=
NM_003494.4:c.4510-331A= MANE Plus Clinical NP_003485.1:n.4510-331A=