Canonical Allele Identifier: CA1335312200

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539827_232539828delinsTG , CM000664.2:g.232539827_232539828delinsTG	GRCh38
NC_000002.11:g.233404537_233404538delinsTG , CM000664.1:g.233404537_233404538delinsTG	GRCh37
NC_000002.10:g.233112781_233112782delinsTG	NCBI36
NG_012954.1:g.5101_5102delinsTG
NG_012954.2:g.5136_5137delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.55+25_55+26delinsTG MANE Select	ENSP00000498757.1:n.55+25_55+26delinsTG
ENST00000389492.3:c.55+25_55+26delinsTG	ENSP00000374143.3:n.55+25_55+26delinsTG
ENST00000389494.7:c.55+25_55+26delinsTG	ENSP00000374145.3:n.55+25_55+26delinsTG
ENST00000485094.1:n.76+25_76+26delinsTG
NM_005199.4:c.55+25_55+26delinsTG	NP_005190.4:n.55+25_55+26delinsTG
NM_005199.5:c.55+25_55+26delinsTG MANE Select	NP_005190.4:n.55+25_55+26delinsTG