Canonical Allele Identifier: CA1732753091

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695958T= , CM000669.2:g.107695958T=	GRCh38
NC_000007.13:g.107336403T= , CM000669.1:g.107336403T=	GRCh37
NC_000007.12:g.107123639T=	NCBI36
NG_008489.1:g.40324T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1463T= MANE Select	ENSP00000494017.1:p.Val488=
ENST00000644846.1:c.174T=
ENST00000265715.7:c.1463T=	ENSP00000265715.3:p.Val488=
ENST00000460748.1:n.566T=
ENST00000477350.5:n.310T=
ENST00000480841.5:n.312T=
ENST00000497446.5:n.478T=
NM_000441.1:c.1463T=	NP_000432.1:p.Val488=
XM_005250425.1:c.1463T=	XP_005250482.1:p.Val488=
XM_005250425.2:c.1463T=	XP_005250482.1:p.Val488=
XM_017012318.1:c.1385T=	XP_016867807.1:p.Val462=
NM_000441.2:c.1463T= MANE Select	NP_000432.1:p.Val488=