Canonical Allele Identifier: CA1732751559

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694567T= , CM000669.2:g.107694567T=	GRCh38
NC_000007.13:g.107335012T= , CM000669.1:g.107335012T=	GRCh37
NC_000007.12:g.107122248T=	NCBI36
NG_008489.1:g.38933T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1342-54T= MANE Select	ENSP00000494017.1:n.1342-54T=
ENST00000644846.1:c.53-54T=
ENST00000265715.7:c.1342-54T=	ENSP00000265715.3:n.1342-54T=
ENST00000460748.1:n.445-54T=
ENST00000477350.5:n.189-54T=
ENST00000480841.5:n.191-54T=
ENST00000497446.5:n.357-54T=
NM_000441.1:c.1342-54T=	NP_000432.1:n.1342-54T=
XM_005250425.1:c.1342-54T=	XP_005250482.1:n.1342-54T=
XM_005250425.2:c.1342-54T=	XP_005250482.1:n.1342-54T=
XM_017012318.1:c.1264-54T=	XP_016867807.1:n.1264-54T=
NM_000441.2:c.1342-54T= MANE Select	NP_000432.1:n.1342-54T=