Canonical Allele Identifier: CA1732751563

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694570C= , CM000669.2:g.107694570C=	GRCh38
NC_000007.13:g.107335015C= , CM000669.1:g.107335015C=	GRCh37
NC_000007.12:g.107122251C=	NCBI36
NG_008489.1:g.38936C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1342-51C= MANE Select	ENSP00000494017.1:n.1342-51C=
ENST00000644846.1:c.53-51C=
ENST00000265715.7:c.1342-51C=	ENSP00000265715.3:n.1342-51C=
ENST00000460748.1:n.445-51C=
ENST00000477350.5:n.189-51C=
ENST00000480841.5:n.191-51C=
ENST00000497446.5:n.357-51C=
NM_000441.1:c.1342-51C=	NP_000432.1:n.1342-51C=
XM_005250425.1:c.1342-51C=	XP_005250482.1:n.1342-51C=
XM_005250425.2:c.1342-51C=	XP_005250482.1:n.1342-51C=
XM_017012318.1:c.1264-51C=	XP_016867807.1:n.1264-51C=
NM_000441.2:c.1342-51C= MANE Select	NP_000432.1:n.1342-51C=