Canonical Allele Identifier: CA2629793209

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595890-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595890G>A , CM000677.2:g.78595890G>A	GRCh38
NC_000015.9:g.78888232G>A , CM000677.1:g.78888232G>A	GRCh37
NC_000015.8:g.76675287G>A	NCBI36
NG_016143.1:g.30406C>T
NG_023328.1:g.35371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*714C>T MANE Select	ENSP00000315602.5:n.*714C>T
ENST00000326828.5:c.*714C>T	ENSP00000315602.5:n.*714C>T
ENST00000348639.7:c.1390-2699C>T	ENSP00000267951.4:n.1390-2699C>T
ENST00000559002.5:n.193+650C>T
ENST00000559658.5:c.*64+650C>T	ENSP00000452896.1:n.*64+650C>T
NM_000743.4:c.*714C>T	NP_000734.2:n.*714C>T
NM_001166694.1:c.1390-2699C>T	NP_001160166.1:n.1390-2699C>T
NR_046313.1:n.2083+650C>T
XM_006720382.1:c.*714C>T	XP_006720445.1:n.*714C>T
XM_011521173.1:c.*714C>T	XP_011519475.1:n.*714C>T
XM_006720382.3:c.*714C>T	XP_006720445.1:n.*714C>T
NM_000743.5:c.*714C>T MANE Select	NP_000734.2:n.*714C>T
NM_001166694.2:c.1390-2699C>T	NP_001160166.1:n.1390-2699C>T
NR_046313.2:n.1784+650C>T