Canonical Allele Identifier: CA1732751359
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710146T= , CM000669.2:g.107710146T= GRCh38
NC_000007.13:g.107350591T= , CM000669.1:g.107350591T= GRCh37
NC_000007.12:g.107137827T= NCBI36
NG_008489.1:g.54512T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2182T= MANE Select ENSP00000494017.1:p.Tyr728=
ENST00000644846.1:c.838T=
ENST00000265715.7:c.2182T= ENSP00000265715.3:p.Tyr728=
ENST00000492030.2:n.377-9T=
NM_000441.1:c.2182T= NP_000432.1:p.Tyr728=
XM_005250425.1:c.2182T= XP_005250482.1:p.Tyr728=
XM_005250425.2:c.2182T= XP_005250482.1:p.Tyr728=
XM_017012318.1:c.2104T= XP_016867807.1:p.Tyr702=
NM_000441.2:c.2182T= MANE Select NP_000432.1:p.Tyr728=