Canonical Allele Identifier: CA2578449460

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978394-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978394C>A , CM000667.2:g.149978394C>A	GRCh38
NC_000005.9:g.149357957C>A , CM000667.1:g.149357957C>A	GRCh37
NC_000005.8:g.149338150C>A	NCBI36
NG_007147.2:g.19512C>A , LRG_684:g.19512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.974C>A
ENST00000286298.5:c.699+43C>A MANE Select	ENSP00000286298.4:n.699+43C>A
ENST00000286298.4:c.699+43C>A	ENSP00000286298.4:n.699+43C>A
ENST00000503336.1:c.372+43C>A	ENSP00000426053.1:n.372+43C>A
NM_000112.3:c.699+43C>A , LRG_684t1:c.699+43C>A	NP_000103.2:n.699+43C>A
XM_017009191.2:c.699+43C>A	XP_016864680.1:n.699+43C>A
NM_000112.4:c.699+43C>A MANE Select	NP_000103.2:n.699+43C>A