Canonical Allele Identifier: CA1590737605

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978587A= , CM000667.2:g.149978587A=	GRCh38
NC_000005.9:g.149358150A= , CM000667.1:g.149358150A=	GRCh37
NC_000005.8:g.149338343A=	NCBI36
NG_007147.2:g.19705A= , LRG_684:g.19705A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1167A=
ENST00000286298.5:c.699+236A= MANE Select	ENSP00000286298.4:n.699+236A=
ENST00000286298.4:c.699+236A=	ENSP00000286298.4:n.699+236A=
ENST00000503336.1:c.372+236A=	ENSP00000426053.1:n.372+236A=
NM_000112.3:c.699+236A= , LRG_684t1:c.699+236A=	NP_000103.2:n.699+236A=
XM_017009191.2:c.699+236A=	XP_016864680.1:n.699+236A=
NM_000112.4:c.699+236A= MANE Select	NP_000103.2:n.699+236A=