Canonical Allele Identifier: CA1335316796

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541555_232541557delinsAAG , CM000664.2:g.232541555_232541557delinsAAG	GRCh38
NC_000002.11:g.233406265_233406267delinsAAG , CM000664.1:g.233406265_233406267delinsAAG	GRCh37
NC_000002.10:g.233114509_233114511delinsAAG	NCBI36
NG_012954.1:g.6829_6831delinsAAG
NG_012954.2:g.6864_6866delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+26_506+28delinsAAG MANE Select	ENSP00000498757.1:n.506+26_506+28delinsAAG
ENST00000389492.3:c.350+844_350+846delinsAAG	ENSP00000374143.3:n.350+844_350+846delinsAAG
ENST00000389494.7:c.506+26_506+28delinsAAG	ENSP00000374145.3:n.506+26_506+28delinsAAG
ENST00000485094.1:n.553_555delinsAAG
NM_005199.4:c.506+26_506+28delinsAAG	NP_005190.4:n.506+26_506+28delinsAAG
NM_005199.5:c.506+26_506+28delinsAAG MANE Select	NP_005190.4:n.506+26_506+28delinsAAG