Canonical Allele Identifier: CA1732759228

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701928G= , CM000669.2:g.107701928G=	GRCh38
NC_000007.13:g.107342373G= , CM000669.1:g.107342373G=	GRCh37
NC_000007.12:g.107129609G=	NCBI36
NG_008489.1:g.46294G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1905G= MANE Select	ENSP00000494017.1:p.Glu635=
ENST00000644846.1:c.616G=
ENST00000265715.7:c.1905G=	ENSP00000265715.3:p.Glu635=
ENST00000492030.2:n.192G=
NM_000441.1:c.1905G=	NP_000432.1:p.Glu635=
XM_005250425.1:c.1905G=	XP_005250482.1:p.Glu635=
XM_005250425.2:c.1905G=	XP_005250482.1:p.Glu635=
XM_017012318.1:c.1827G=	XP_016867807.1:p.Glu609=
NM_000441.2:c.1905G= MANE Select	NP_000432.1:p.Glu635=