Canonical Allele Identifier: CA2663623654

Gene: CHRNG

Linked Data

• gnomAD v4: 2-232541601-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541604del , CM000664.2:g.232541604del	GRCh38
NC_000002.11:g.233406314del , CM000664.1:g.233406314del	GRCh37
NC_000002.10:g.233114558del	NCBI36
NG_012954.1:g.6878del
NG_012954.2:g.6913del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+75del MANE Select	ENSP00000498757.1:n.506+75del
ENST00000389492.3:c.351-819del	ENSP00000374143.3:n.351-819del
ENST00000389494.7:c.506+75del	ENSP00000374145.3:n.506+75del
ENST00000485094.1:n.602del
NM_005199.4:c.506+75del	NP_005190.4:n.506+75del
NM_005199.5:c.506+75del MANE Select	NP_005190.4:n.506+75del