Canonical Allele Identifier: CA2250850295
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145889C= , CM000679.2:g.18145889C= GRCh38
NC_000017.10:g.18049203C= , CM000679.1:g.18049203C= GRCh37
NC_000017.9:g.17989928C= NCBI36
NG_011634.1:g.42184C=
NG_011634.2:g.42184C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6291C= MANE Select ENSP00000495481.1:p.Gly2097=
ENST00000205890.9:c.6291C= ENSP00000205890.5:p.Gly2097=
ENST00000615845.4:c.6291C= ENSP00000481642.1:p.Gly2097=
NM_016239.3:c.6291C= NP_057323.3:p.Gly2097=
XM_011523917.1:c.6231C= XP_011522219.1:p.Gly2077=
XM_011523918.1:c.6231C= XP_011522220.1:p.Gly2077=
XM_011523921.1:c.6285C= XP_011522223.1:p.Gly2095=
XR_934037.1:n.6890C=
XR_934038.1:n.6890C=
XM_011523918.2:c.6231C= XP_011522220.1:p.Gly2077=
XM_017024714.2:c.6231C= XP_016880203.1:p.Gly2077=
XM_017024715.2:c.6294C= XP_016880204.1:p.Gly2098=
XM_024450781.1:c.6213+1297C= XP_024306549.1:n.6213+1297C=
NM_016239.4:c.6291C= MANE Select NP_057323.3:p.Gly2097=