Canonical Allele Identifier: CA263260

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149977983G>T , CM000667.2:g.149977983G>T	GRCh38
NC_000005.9:g.149357546G>T , CM000667.1:g.149357546G>T	GRCh37
NC_000005.8:g.149337739G>T	NCBI36
NG_007147.2:g.19101G>T , LRG_684:g.19101G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000112.4:c.331G>T MANE Select	NP_000103.2:p.Asp111Tyr
ENST00000286298.5:c.331G>T MANE Select	ENSP00000286298.4:p.Asp111Tyr
NM_000112.3:c.331G>T , LRG_684t1:c.331G>T	NP_000103.2:p.Asp111Tyr
ENST00000286298.4:c.331G>T	ENSP00000286298.4:p.Asp111Tyr
ENST00000503336.1:c.4G>T	ENSP00000426053.1:p.Asp2Tyr
ENST00000690410.1:n.563G>T
XM_017009191.2:c.331G>T	XP_016864680.1:p.Asp111Tyr