Canonical Allele Identifier: CA1590738976

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981855_149981856delinsAT , CM000667.2:g.149981855_149981856delinsAT	GRCh38
NC_000005.9:g.149361418_149361419delinsAT , CM000667.1:g.149361418_149361419delinsAT	GRCh37
NC_000005.8:g.149341611_149341612delinsAT	NCBI36
NG_007147.2:g.22973_22974delinsAT , LRG_684:g.22973_22974delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*42_*43delinsAT MANE Select	ENSP00000286298.4:n.*42_*43delinsAT
ENST00000286298.4:c.*42_*43delinsAT	ENSP00000286298.4:n.*42_*43delinsAT
ENST00000503336.1:c.372+3504_372+3505delinsAT	ENSP00000426053.1:n.372+3504_372+3505delinsAT
NM_000112.3:c.*42_*43delinsAT , LRG_684t1:c.*42_*43delinsAT	NP_000103.2:n.*42_*43delinsAT
XM_017009191.2:c.*12+30_*12+31delinsAT	XP_016864680.1:n.*12+30_*12+31delinsAT
NM_000112.4:c.*42_*43delinsAT MANE Select	NP_000103.2:n.*42_*43delinsAT