Canonical Allele Identifier: CA1732761821

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107704385G= , CM000669.2:g.107704385G=	GRCh38
NC_000007.13:g.107344830G= , CM000669.1:g.107344830G=	GRCh37
NC_000007.12:g.107132066G=	NCBI36
NG_008489.1:g.48751G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.2089G= MANE Select	ENSP00000494017.1:p.Asp697=
ENST00000644846.1:c.745+2328G=
ENST00000265715.7:c.2089G=	ENSP00000265715.3:p.Asp697=
ENST00000492030.2:n.376G=
NM_000441.1:c.2089G=	NP_000432.1:p.Asp697=
XM_005250425.1:c.2089G=	XP_005250482.1:p.Asp697=
XM_005250425.2:c.2089G=	XP_005250482.1:p.Asp697=
XM_017012318.1:c.2011G=	XP_016867807.1:p.Asp671=
NM_000441.2:c.2089G= MANE Select	NP_000432.1:p.Asp697=