Canonical Allele Identifier: CA1590737432

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978159C= , CM000667.2:g.149978159C=	GRCh38
NC_000005.9:g.149357722C= , CM000667.1:g.149357722C=	GRCh37
NC_000005.8:g.149337915C=	NCBI36
NG_007147.2:g.19277C= , LRG_684:g.19277C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000690410.1:n.739C=
ENST00000286298.5:c.507C= MANE Select	ENSP00000286298.4:p.Cys169=
ENST00000286298.4:c.507C=	ENSP00000286298.4:p.Cys169=
ENST00000503336.1:c.180C=	ENSP00000426053.1:p.Cys60=
NM_000112.3:c.507C= , LRG_684t1:c.507C=	NP_000103.2:p.Cys169=
XM_017009191.2:c.507C=	XP_016864680.1:p.Cys169=
NM_000112.4:c.507C= MANE Select	NP_000103.2:p.Cys169=