Canonical Allele Identifier: CA2189598993

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595874A= , CM000677.2:g.78595874A=	GRCh38
NC_000015.9:g.78888216A= , CM000677.1:g.78888216A=	GRCh37
NC_000015.8:g.76675271A=	NCBI36
NG_016143.1:g.30422T=
NG_023328.1:g.35355A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*730T= MANE Select	ENSP00000315602.5:n.*730T=
ENST00000326828.5:c.*730T=	ENSP00000315602.5:n.*730T=
ENST00000348639.7:c.1390-2683T=	ENSP00000267951.4:n.1390-2683T=
ENST00000559002.5:n.193+666T=
ENST00000559658.5:c.*64+666T=	ENSP00000452896.1:n.*64+666T=
NM_000743.4:c.*730T=	NP_000734.2:n.*730T=
NM_001166694.1:c.1390-2683T=	NP_001160166.1:n.1390-2683T=
NR_046313.1:n.2083+666T=
XM_006720382.1:c.*730T=	XP_006720445.1:n.*730T=
XM_011521173.1:c.*730T=	XP_011519475.1:n.*730T=
XM_006720382.3:c.*730T=	XP_006720445.1:n.*730T=
NM_000743.5:c.*730T= MANE Select	NP_000734.2:n.*730T=
NM_001166694.2:c.1390-2683T=	NP_001160166.1:n.1390-2683T=
NR_046313.2:n.1784+666T=