Canonical Allele Identifier: CA2675943528

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978445-A-AGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978445_149978446insGTT , CM000667.2:g.149978445_149978446insGTT	GRCh38
NC_000005.9:g.149358008_149358009insGTT , CM000667.1:g.149358008_149358009insGTT	GRCh37
NC_000005.8:g.149338201_149338202insGTT	NCBI36
NG_007147.2:g.19563_19564insGTT , LRG_684:g.19563_19564insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1025_1026insGTT
ENST00000286298.5:c.699+94_699+95insGTT MANE Select	ENSP00000286298.4:n.699+94_699+95insGTT
ENST00000286298.4:c.699+94_699+95insGTT	ENSP00000286298.4:n.699+94_699+95insGTT
ENST00000503336.1:c.372+94_372+95insGTT	ENSP00000426053.1:n.372+94_372+95insGTT
NM_000112.3:c.699+94_699+95insGTT , LRG_684t1:c.699+94_699+95insGTT	NP_000103.2:n.699+94_699+95insGTT
XM_017009191.2:c.699+94_699+95insGTT	XP_016864680.1:n.699+94_699+95insGTT
NM_000112.4:c.699+94_699+95insGTT MANE Select	NP_000103.2:n.699+94_699+95insGTT