Canonical Allele Identifier: CA1732751861

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694718T= , CM000669.2:g.107694718T=	GRCh38
NC_000007.13:g.107335163T= , CM000669.1:g.107335163T=	GRCh37
NC_000007.12:g.107122399T=	NCBI36
NG_008489.1:g.39084T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000441.2:c.1437+2T= MANE Select	NP_000432.1:n.1437+2T=
ENST00000644269.2:c.1437+2T= MANE Select	ENSP00000494017.1:n.1437+2T=
NM_000441.1:c.1437+2T=	NP_000432.1:n.1437+2T=
ENST00000265715.7:c.1437+2T=	ENSP00000265715.3:n.1437+2T=
ENST00000460748.1:n.540+2T=
ENST00000477350.5:n.284+2T=
ENST00000480841.5:n.286+2T=
ENST00000497446.5:n.452+2T=
ENST00000644846.1:c.148+2T=
XM_005250425.1:c.1437+2T=	XP_005250482.1:n.1437+2T=
XM_005250425.2:c.1437+2T=	XP_005250482.1:n.1437+2T=
XM_017012318.1:c.1359+2T=	XP_016867807.1:n.1359+2T=