Canonical Allele Identifier: CA1732759169

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701888A= , CM000669.2:g.107701888A=	GRCh38
NC_000007.13:g.107342333A= , CM000669.1:g.107342333A=	GRCh37
NC_000007.12:g.107129569A=	NCBI36
NG_008489.1:g.46254A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1865A= MANE Select	ENSP00000494017.1:p.Glu622=
ENST00000644846.1:c.576A=
ENST00000265715.7:c.1865A=	ENSP00000265715.3:p.Glu622=
ENST00000492030.2:n.152A=
NM_000441.1:c.1865A=	NP_000432.1:p.Glu622=
XM_005250425.1:c.1865A=	XP_005250482.1:p.Glu622=
XM_005250425.2:c.1865A=	XP_005250482.1:p.Glu622=
XM_017012318.1:c.1787A=	XP_016867807.1:p.Glu596=
NM_000441.2:c.1865A= MANE Select	NP_000432.1:p.Glu622=