Canonical Allele Identifier: CA2550474415
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107688933_107688934insTAATCAGAAGTTGGT , CM000669.2:g.107688933_107688934insTAATCAGAAGTTGGT GRCh38
NC_000007.13:g.107329378_107329379insTAATCAGAAGTTGGT , CM000669.1:g.107329378_107329379insTAATCAGAAGTTGGT GRCh37
NC_000007.12:g.107116614_107116615insTAATCAGAAGTTGGT NCBI36
NG_008489.1:g.33299_33300insTAATCAGAAGTTGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1002-120_1002-119insTAATCAGAAGTTGGT MANE Select ENSP00000494017.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
ENST00000265715.7:c.1002-120_1002-119insTAATCAGAAGTTGGT ENSP00000265715.3:n.1002-120_1002-119insTAATCAGAAGTTGGT
NM_000441.1:c.1002-120_1002-119insTAATCAGAAGTTGGT NP_000432.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
XM_005250425.1:c.1002-120_1002-119insTAATCAGAAGTTGGT XP_005250482.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
XM_006716025.2:c.1002-120_1002-119insTAATCAGAAGTTGGT XP_006716088.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
XM_005250425.2:c.1002-120_1002-119insTAATCAGAAGTTGGT XP_005250482.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
XM_006716025.3:c.1002-120_1002-119insTAATCAGAAGTTGGT XP_006716088.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
XM_017012318.1:c.1002-120_1002-119insTAATCAGAAGTTGGT XP_016867807.1:n.1002-120_1002-119insTAATCAGAAGTTGGT
NM_000441.2:c.1002-120_1002-119insTAATCAGAAGTTGGT MANE Select NP_000432.1:n.1002-120_1002-119insTAATCAGAAGTTGGT