Canonical Allele Identifier: CA2675943522

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978433-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978434_149978435insTT , CM000667.2:g.149978434_149978435insTT	GRCh38
NC_000005.9:g.149357997_149357998insTT , CM000667.1:g.149357997_149357998insTT	GRCh37
NC_000005.8:g.149338190_149338191insTT	NCBI36
NG_007147.2:g.19552_19553insTT , LRG_684:g.19552_19553insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1014_1015insTT
ENST00000286298.5:c.699+83_699+84insTT MANE Select	ENSP00000286298.4:n.699+83_699+84insTT
ENST00000286298.4:c.699+83_699+84insTT	ENSP00000286298.4:n.699+83_699+84insTT
ENST00000503336.1:c.372+83_372+84insTT	ENSP00000426053.1:n.372+83_372+84insTT
NM_000112.3:c.699+83_699+84insTT , LRG_684t1:c.699+83_699+84insTT	NP_000103.2:n.699+83_699+84insTT
XM_017009191.2:c.699+83_699+84insTT	XP_016864680.1:n.699+83_699+84insTT
NM_000112.4:c.699+83_699+84insTT MANE Select	NP_000103.2:n.699+83_699+84insTT