Canonical Allele Identifier: CA1732755291

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107698076A= , CM000669.2:g.107698076A=	GRCh38
NC_000007.13:g.107338521A= , CM000669.1:g.107338521A=	GRCh37
NC_000007.12:g.107125757A=	NCBI36
NG_008489.1:g.42442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1579A= MANE Select	ENSP00000494017.1:p.Thr527=
ENST00000644846.1:c.290A=
ENST00000265715.7:c.1579A=	ENSP00000265715.3:p.Thr527=
ENST00000477350.5:n.426A=
ENST00000480841.5:n.428A=
NM_000441.1:c.1579A=	NP_000432.1:p.Thr527=
XM_005250425.1:c.1579A=	XP_005250482.1:p.Thr527=
XM_005250425.2:c.1579A=	XP_005250482.1:p.Thr527=
XM_017012318.1:c.1501A=	XP_016867807.1:p.Thr501=
NM_000441.2:c.1579A= MANE Select	NP_000432.1:p.Thr527=