Canonical Allele Identifier: CA2245821913

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454530_7454532delinsATC , CM000679.2:g.7454530_7454532delinsATC	GRCh38
NC_000017.10:g.7357849_7357851delinsATC , CM000679.1:g.7357849_7357851delinsATC	GRCh37
NC_000017.9:g.7298573_7298575delinsATC	NCBI36
NG_008026.1:g.14444_14446delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+10_1044+12delinsATC MANE Select	ENSP00000304290.2:n.1044+10_1044+12delinsATC
ENST00000306071.6:c.1044+10_1044+12delinsATC	ENSP00000304290.2:n.1044+10_1044+12delinsATC
ENST00000536404.6:c.828+10_828+12delinsATC	ENSP00000439209.2:n.828+10_828+12delinsATC
ENST00000570557.5:c.707+10_707+12delinsATC
ENST00000573209.1:n.1988+10_1988+12delinsATC
ENST00000576360.1:c.681+10_681+12delinsATC	ENSP00000459092.1:n.681+10_681+12delinsATC
NM_000747.2:c.1044+10_1044+12delinsATC	NP_000738.2:n.1044+10_1044+12delinsATC
NM_000747.3:c.1044+10_1044+12delinsATC MANE Select	NP_000738.2:n.1044+10_1044+12delinsATC