Canonical Allele Identifier: CA2832547817

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541330dup , CM000664.2:g.232541330dup	GRCh38
NC_000002.11:g.233406040dup , CM000664.1:g.233406040dup	GRCh37
NC_000002.10:g.233114284dup	NCBI36
NG_012954.1:g.6604dup
NG_012954.2:g.6639dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.351-44dup MANE Select	ENSP00000498757.1:n.351-44dup
ENST00000389492.3:c.350+619dup	ENSP00000374143.3:n.350+619dup
ENST00000389494.7:c.351-44dup	ENSP00000374145.3:n.351-44dup
ENST00000485094.1:n.372-44dup
NM_005199.4:c.351-44dup	NP_005190.4:n.351-44dup
NM_005199.5:c.351-44dup MANE Select	NP_005190.4:n.351-44dup