Canonical Allele Identifier: CA1590738982

Gene: SLC26A2

Linked Data

• dbSNP Id: rs1755113521

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981865_149981866dup , CM000667.2:g.149981865_149981866dup	GRCh38
NC_000005.9:g.149361428_149361429dup , CM000667.1:g.149361428_149361429dup	GRCh37
NC_000005.8:g.149341621_149341622dup	NCBI36
NG_007147.2:g.22983_22984dup , LRG_684:g.22983_22984dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*52_*53dup MANE Select	ENSP00000286298.4:n.*52_*53dup
ENST00000286298.4:c.*52_*53dup	ENSP00000286298.4:n.*52_*53dup
ENST00000503336.1:c.372+3514_372+3515dup	ENSP00000426053.1:n.372+3514_372+3515dup
NM_000112.3:c.*52_*53dup , LRG_684t1:c.*52_*53dup	NP_000103.2:n.*52_*53dup
XM_017009191.2:c.*12+40_*12+41dup	XP_016864680.1:n.*12+40_*12+41dup
NM_000112.4:c.*52_*53dup MANE Select	NP_000103.2:n.*52_*53dup