Canonical Allele Identifier: CA1590738355

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980429G= , CM000667.2:g.149980429G=	GRCh38
NC_000005.9:g.149359992G= , CM000667.1:g.149359992G=	GRCh37
NC_000005.8:g.149340185G=	NCBI36
NG_007147.2:g.21547G= , LRG_684:g.21547G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286298.5:c.836G= MANE Select	ENSP00000286298.4:p.Arg279=
ENST00000286298.4:c.836G=	ENSP00000286298.4:p.Arg279=
ENST00000503336.1:c.372+2078G=	ENSP00000426053.1:n.372+2078G=
NM_000112.3:c.836G= , LRG_684t1:c.836G=	NP_000103.2:p.Arg279=
XM_017009191.2:c.836G=	XP_016864680.1:p.Arg279=
NM_000112.4:c.836G= MANE Select	NP_000103.2:p.Arg279=