Canonical Allele Identifier: CA1590737590

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978552_149978553delinsAC , CM000667.2:g.149978552_149978553delinsAC	GRCh38
NC_000005.9:g.149358115_149358116delinsAC , CM000667.1:g.149358115_149358116delinsAC	GRCh37
NC_000005.8:g.149338308_149338309delinsAC	NCBI36
NG_007147.2:g.19670_19671delinsAC , LRG_684:g.19670_19671delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.1132_1133delinsAC
ENST00000286298.5:c.699+201_699+202delinsAC MANE Select	ENSP00000286298.4:n.699+201_699+202delinsAC
ENST00000286298.4:c.699+201_699+202delinsAC	ENSP00000286298.4:n.699+201_699+202delinsAC
ENST00000503336.1:c.372+201_372+202delinsAC	ENSP00000426053.1:n.372+201_372+202delinsAC
NM_000112.3:c.699+201_699+202delinsAC , LRG_684t1:c.699+201_699+202delinsAC	NP_000103.2:n.699+201_699+202delinsAC
XM_017009191.2:c.699+201_699+202delinsAC	XP_016864680.1:n.699+201_699+202delinsAC
NM_000112.4:c.699+201_699+202delinsAC MANE Select	NP_000103.2:n.699+201_699+202delinsAC