Canonical Allele Identifier: CA2561249664
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107688929_107688930insATAA , CM000669.2:g.107688929_107688930insATAA GRCh38
NC_000007.13:g.107329374_107329375insATAA , CM000669.1:g.107329374_107329375insATAA GRCh37
NC_000007.12:g.107116610_107116611insATAA NCBI36
NG_008489.1:g.33295_33296insATAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1002-124_1002-123insATAA MANE Select ENSP00000494017.1:n.1002-124_1002-123insATAA
ENST00000265715.7:c.1002-124_1002-123insATAA ENSP00000265715.3:n.1002-124_1002-123insATAA
NM_000441.1:c.1002-124_1002-123insATAA NP_000432.1:n.1002-124_1002-123insATAA
XM_005250425.1:c.1002-124_1002-123insATAA XP_005250482.1:n.1002-124_1002-123insATAA
XM_006716025.2:c.1002-124_1002-123insATAA XP_006716088.1:n.1002-124_1002-123insATAA
XM_005250425.2:c.1002-124_1002-123insATAA XP_005250482.1:n.1002-124_1002-123insATAA
XM_006716025.3:c.1002-124_1002-123insATAA XP_006716088.1:n.1002-124_1002-123insATAA
XM_017012318.1:c.1002-124_1002-123insATAA XP_016867807.1:n.1002-124_1002-123insATAA
NM_000441.2:c.1002-124_1002-123insATAA MANE Select NP_000432.1:n.1002-124_1002-123insATAA