Canonical Allele Identifier: CA2577278019

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539840del , CM000664.2:g.232539840del	GRCh38
NC_000002.11:g.233404550del , CM000664.1:g.233404550del	GRCh37
NC_000002.10:g.233112794del	NCBI36
NG_012954.1:g.5114del
NG_012954.2:g.5149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+38del MANE Select	ENSP00000498757.1:n.55+38del
ENST00000389492.3:c.55+38del	ENSP00000374143.3:n.55+38del
ENST00000389494.7:c.55+38del	ENSP00000374145.3:n.55+38del
ENST00000485094.1:n.76+38del
NM_005199.4:c.55+38del	NP_005190.4:n.55+38del
NM_005199.5:c.55+38del MANE Select	NP_005190.4:n.55+38del