Canonical Allele Identifier: CA1732753126

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695986T= , CM000669.2:g.107695986T=	GRCh38
NC_000007.13:g.107336431T= , CM000669.1:g.107336431T=	GRCh37
NC_000007.12:g.107123667T=	NCBI36
NG_008489.1:g.40352T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1491T= MANE Select	ENSP00000494017.1:p.Gly497=
ENST00000644846.1:c.202T=
ENST00000265715.7:c.1491T=	ENSP00000265715.3:p.Gly497=
ENST00000477350.5:n.338T=
ENST00000480841.5:n.340T=
ENST00000497446.5:n.506T=
NM_000441.1:c.1491T=	NP_000432.1:p.Gly497=
XM_005250425.1:c.1491T=	XP_005250482.1:p.Gly497=
XM_005250425.2:c.1491T=	XP_005250482.1:p.Gly497=
XM_017012318.1:c.1413T=	XP_016867807.1:p.Gly471=
NM_000441.2:c.1491T= MANE Select	NP_000432.1:p.Gly497=