Canonical Allele Identifier: CA4433053
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs145805875

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710095G>T , CM000669.2:g.107710095G>T GRCh38
NC_000007.13:g.107350540G>T , CM000669.1:g.107350540G>T GRCh37
NC_000007.12:g.107137776G>T NCBI36
NG_008489.1:g.54461G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2131G>T MANE Select ENSP00000494017.1:p.Asp711Tyr
ENST00000644846.1:c.787G>T
ENST00000265715.7:c.2131G>T ENSP00000265715.3:p.Asp711Tyr
ENST00000492030.2:n.377-60G>T
NM_000441.1:c.2131G>T NP_000432.1:p.Asp711Tyr
XM_005250425.1:c.2131G>T XP_005250482.1:p.Asp711Tyr
XM_005250425.2:c.2131G>T XP_005250482.1:p.Asp711Tyr
XM_017012318.1:c.2053G>T XP_016867807.1:p.Asp685Tyr
NM_000441.2:c.2131G>T MANE Select NP_000432.1:p.Asp711Tyr