Canonical Allele Identifier: CA2675943561

Gene: SLC26A2

Linked Data

• gnomAD v4: 5-149978501-C-CTGGGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978501_149978502insTGGGGCA , CM000667.2:g.149978501_149978502insTGGGGCA	GRCh38
NC_000005.9:g.149358064_149358065insTGGGGCA , CM000667.1:g.149358064_149358065insTGGGGCA	GRCh37
NC_000005.8:g.149338257_149338258insTGGGGCA	NCBI36
NG_007147.2:g.19619_19620insTGGGGCA , LRG_684:g.19619_19620insTGGGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1081_1082insTGGGGCA
ENST00000286298.5:c.699+150_699+151insTGGGGCA MANE Select	ENSP00000286298.4:n.699+150_699+151insTGGGGCA
ENST00000286298.4:c.699+150_699+151insTGGGGCA	ENSP00000286298.4:n.699+150_699+151insTGGGGCA
ENST00000503336.1:c.372+150_372+151insTGGGGCA	ENSP00000426053.1:n.372+150_372+151insTGGGGCA
NM_000112.3:c.699+150_699+151insTGGGGCA , LRG_684t1:c.699+150_699+151insTGGGGCA	NP_000103.2:n.699+150_699+151insTGGGGCA
XM_017009191.2:c.699+150_699+151insTGGGGCA	XP_016864680.1:n.699+150_699+151insTGGGGCA
NM_000112.4:c.699+150_699+151insTGGGGCA MANE Select	NP_000103.2:n.699+150_699+151insTGGGGCA