Canonical Allele Identifier: CA2629793441

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595959-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595959C>A , CM000677.2:g.78595959C>A	GRCh38
NC_000015.9:g.78888301C>A , CM000677.1:g.78888301C>A	GRCh37
NC_000015.8:g.76675356C>A	NCBI36
NG_016143.1:g.30337G>T
NG_023328.1:g.35440C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*645G>T MANE Select	ENSP00000315602.5:n.*645G>T
ENST00000326828.5:c.*645G>T	ENSP00000315602.5:n.*645G>T
ENST00000348639.7:c.1390-2768G>T	ENSP00000267951.4:n.1390-2768G>T
ENST00000559002.5:n.193+581G>T
ENST00000559658.5:c.*64+581G>T	ENSP00000452896.1:n.*64+581G>T
NM_000743.4:c.*645G>T	NP_000734.2:n.*645G>T
NM_001166694.1:c.1390-2768G>T	NP_001160166.1:n.1390-2768G>T
NR_046313.1:n.2083+581G>T
XM_006720382.1:c.*645G>T	XP_006720445.1:n.*645G>T
XM_011521173.1:c.*645G>T	XP_011519475.1:n.*645G>T
XM_006720382.3:c.*645G>T	XP_006720445.1:n.*645G>T
NM_000743.5:c.*645G>T MANE Select	NP_000734.2:n.*645G>T
NM_001166694.2:c.1390-2768G>T	NP_001160166.1:n.1390-2768G>T
NR_046313.2:n.1784+581G>T