Canonical Allele Identifier: CA1732751410
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107694470C= , CM000669.2:g.107694470C= GRCh38
NC_000007.13:g.107334915C= , CM000669.1:g.107334915C= GRCh37
NC_000007.12:g.107122151C= NCBI36
NG_008489.1:g.38836C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1331C= MANE Select ENSP00000494017.1:p.Pro444=
ENST00000644846.1:c.42C=
ENST00000265715.7:c.1331C= ENSP00000265715.3:p.Pro444=
ENST00000460748.1:n.434C=
ENST00000477350.5:n.189-151C=
ENST00000480841.5:n.180C=
ENST00000497446.5:n.346C=
NM_000441.1:c.1331C= NP_000432.1:p.Pro444=
XM_005250425.1:c.1331C= XP_005250482.1:p.Pro444=
XM_005250425.2:c.1331C= XP_005250482.1:p.Pro444=
XM_017012318.1:c.1264-151C= XP_016867807.1:n.1264-151C=
NM_000441.2:c.1331C= MANE Select NP_000432.1:p.Pro444=