Canonical Allele Identifier: CA2768880014

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978583G>A , CM000667.2:g.149978583G>A	GRCh38
NC_000005.9:g.149358146G>A , CM000667.1:g.149358146G>A	GRCh37
NC_000005.8:g.149338339G>A	NCBI36
NG_007147.2:g.19701G>A , LRG_684:g.19701G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1163G>A
ENST00000286298.5:c.699+232G>A MANE Select	ENSP00000286298.4:n.699+232G>A
ENST00000286298.4:c.699+232G>A	ENSP00000286298.4:n.699+232G>A
ENST00000503336.1:c.372+232G>A	ENSP00000426053.1:n.372+232G>A
NM_000112.3:c.699+232G>A , LRG_684t1:c.699+232G>A	NP_000103.2:n.699+232G>A
XM_017009191.2:c.699+232G>A	XP_016864680.1:n.699+232G>A
NM_000112.4:c.699+232G>A MANE Select	NP_000103.2:n.699+232G>A