Canonical Allele Identifier: CA1590738960

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981827_149981830delinsTAGA , CM000667.2:g.149981827_149981830delinsTAGA	GRCh38
NC_000005.9:g.149361390_149361393delinsTAGA , CM000667.1:g.149361390_149361393delinsTAGA	GRCh37
NC_000005.8:g.149341583_149341586delinsTAGA	NCBI36
NG_007147.2:g.22945_22948delinsTAGA , LRG_684:g.22945_22948delinsTAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*14_*17delinsTAGA MANE Select	ENSP00000286298.4:n.*14_*17delinsTAGA
ENST00000286298.4:c.*14_*17delinsTAGA	ENSP00000286298.4:n.*14_*17delinsTAGA
ENST00000503336.1:c.372+3476_372+3479delinsTAGA	ENSP00000426053.1:n.372+3476_372+3479delinsTAGA
NM_000112.3:c.*14_*17delinsTAGA , LRG_684t1:c.*14_*17delinsTAGA	NP_000103.2:n.*14_*17delinsTAGA
XM_017009191.2:c.*12+2_*12+5delinsTAGA	XP_016864680.1:n.*12+2_*12+5delinsTAGA
NM_000112.4:c.*14_*17delinsTAGA MANE Select	NP_000103.2:n.*14_*17delinsTAGA