Canonical Allele Identifier: CA1590738928

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981752A= , CM000667.2:g.149981752A=	GRCh38
NC_000005.9:g.149361315A= , CM000667.1:g.149361315A=	GRCh37
NC_000005.8:g.149341508A=	NCBI36
NG_007147.2:g.22870A= , LRG_684:g.22870A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.2159A= MANE Select	ENSP00000286298.4:p.Glu720=
ENST00000286298.4:c.2159A=	ENSP00000286298.4:p.Glu720=
ENST00000503336.1:c.372+3401A=	ENSP00000426053.1:n.372+3401A=
NM_000112.3:c.2159A= , LRG_684t1:c.2159A=	NP_000103.2:p.Glu720=
XM_017009191.2:c.2159A=	XP_016864680.1:p.Glu720=
NM_000112.4:c.2159A= MANE Select	NP_000103.2:p.Glu720=