Canonical Allele Identifier: CA1590737610

Gene: SLC26A2

Linked Data

• dbSNP Id: rs1755038883

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978604_149978608del , CM000667.2:g.149978604_149978608del	GRCh38
NC_000005.9:g.149358167_149358171del , CM000667.1:g.149358167_149358171del	GRCh37
NC_000005.8:g.149338360_149338364del	NCBI36
NG_007147.2:g.19722_19726del , LRG_684:g.19722_19726del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1184_1188del
ENST00000286298.5:c.699+253_699+257del MANE Select	ENSP00000286298.4:n.699+253_699+257del
ENST00000286298.4:c.699+253_699+257del	ENSP00000286298.4:n.699+253_699+257del
ENST00000503336.1:c.372+253_372+257del	ENSP00000426053.1:n.372+253_372+257del
NM_000112.3:c.699+253_699+257del , LRG_684t1:c.699+253_699+257del	NP_000103.2:n.699+253_699+257del
XM_017009191.2:c.699+253_699+257del	XP_016864680.1:n.699+253_699+257del
NM_000112.4:c.699+253_699+257del MANE Select	NP_000103.2:n.699+253_699+257del