Canonical Allele Identifier: CA2245821925

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454547_7454548delinsCA , CM000679.2:g.7454547_7454548delinsCA	GRCh38
NC_000017.10:g.7357866_7357867delinsCA , CM000679.1:g.7357866_7357867delinsCA	GRCh37
NC_000017.9:g.7298590_7298591delinsCA	NCBI36
NG_008026.1:g.14461_14462delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+27_1044+28delinsCA MANE Select	ENSP00000304290.2:n.1044+27_1044+28delinsCA
ENST00000306071.6:c.1044+27_1044+28delinsCA	ENSP00000304290.2:n.1044+27_1044+28delinsCA
ENST00000536404.6:c.828+27_828+28delinsCA	ENSP00000439209.2:n.828+27_828+28delinsCA
ENST00000570557.5:c.707+27_707+28delinsCA
ENST00000573209.1:n.1988+27_1988+28delinsCA
ENST00000576360.1:c.681+27_681+28delinsCA	ENSP00000459092.1:n.681+27_681+28delinsCA
NM_000747.2:c.1044+27_1044+28delinsCA	NP_000738.2:n.1044+27_1044+28delinsCA
NM_000747.3:c.1044+27_1044+28delinsCA MANE Select	NP_000738.2:n.1044+27_1044+28delinsCA