Canonical Allele Identifier: CA1732751364

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694425C= , CM000669.2:g.107694425C=	GRCh38
NC_000007.13:g.107334870C= , CM000669.1:g.107334870C=	GRCh37
NC_000007.12:g.107122106C=	NCBI36
NG_008489.1:g.38791C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1286C= MANE Select	ENSP00000494017.1:p.Ala429=
ENST00000265715.7:c.1286C=	ENSP00000265715.3:p.Ala429=
ENST00000460748.1:n.389C=
ENST00000477350.5:n.189-196C=
ENST00000480841.5:n.135C=
ENST00000497446.5:n.301C=
NM_000441.1:c.1286C=	NP_000432.1:p.Ala429=
XM_005250425.1:c.1286C=	XP_005250482.1:p.Ala429=
XM_005250425.2:c.1286C=	XP_005250482.1:p.Ala429=
XM_017012318.1:c.1264-196C=	XP_016867807.1:n.1264-196C=
NM_000441.2:c.1286C= MANE Select	NP_000432.1:p.Ala429=