Canonical Allele Identifier: CA1335316841

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541658_232541659delinsCT , CM000664.2:g.232541658_232541659delinsCT	GRCh38
NC_000002.11:g.233406368_233406369delinsCT , CM000664.1:g.233406368_233406369delinsCT	GRCh37
NC_000002.10:g.233114612_233114613delinsCT	NCBI36
NG_012954.1:g.6932_6933delinsCT
NG_012954.2:g.6967_6968delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+129_506+130delinsCT MANE Select	ENSP00000498757.1:n.506+129_506+130delinsCT
ENST00000389492.3:c.351-765_351-764delinsCT	ENSP00000374143.3:n.351-765_351-764delinsCT
ENST00000389494.7:c.506+129_506+130delinsCT	ENSP00000374145.3:n.506+129_506+130delinsCT
ENST00000485094.1:n.656_657delinsCT
NM_005199.4:c.506+129_506+130delinsCT	NP_005190.4:n.506+129_506+130delinsCT
NM_005199.5:c.506+129_506+130delinsCT MANE Select	NP_005190.4:n.506+129_506+130delinsCT