Canonical Allele Identifier: CA1335312232

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539894_232539896delinsCCT , CM000664.2:g.232539894_232539896delinsCCT	GRCh38
NC_000002.11:g.233404604_233404606delinsCCT , CM000664.1:g.233404604_233404606delinsCCT	GRCh37
NC_000002.10:g.233112848_233112850delinsCCT	NCBI36
NG_012954.1:g.5168_5170delinsCCT
NG_012954.2:g.5203_5205delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+92_55+94delinsCCT MANE Select	ENSP00000498757.1:n.55+92_55+94delinsCCT
ENST00000389492.3:c.55+92_55+94delinsCCT	ENSP00000374143.3:n.55+92_55+94delinsCCT
ENST00000389494.7:c.55+92_55+94delinsCCT	ENSP00000374145.3:n.55+92_55+94delinsCCT
ENST00000485094.1:n.76+92_76+94delinsCCT
NM_005199.4:c.55+92_55+94delinsCCT	NP_005190.4:n.55+92_55+94delinsCCT
NM_005199.5:c.55+92_55+94delinsCCT MANE Select	NP_005190.4:n.55+92_55+94delinsCCT