Canonical Allele Identifier: CA2653788338

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63349555-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349555G>T , CM000682.2:g.63349555G>T	GRCh38
NC_000020.10:g.61980907G>T , CM000682.1:g.61980907G>T	GRCh37
NC_000020.9:g.61451351G>T	NCBI36
NG_011931.1:g.16789C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1758+98C>A MANE Select	ENSP00000359285.4:n.1758+98C>A
ENST00000370263.8:c.1758+98C>A	ENSP00000359285.4:n.1758+98C>A
ENST00000463705.5:n.2406+98C>A
ENST00000467563.3:n.1828+98C>A
ENST00000498043.6:c.1782+98C>A
ENST00000615287.4:c.1545+98C>A	ENSP00000483388.1:n.1545+98C>A
ENST00000627000.1:c.*1447+98C>A	ENSP00000486914.1:n.*1447+98C>A
ENST00000630240.1:n.1577C>A
NM_000744.6:c.1758+98C>A	NP_000735.1:n.1758+98C>A
NM_001256573.1:c.1230+98C>A	NP_001243502.1:n.1230+98C>A
NR_046317.1:n.2014+98C>A
XM_011528524.1:c.1545+98C>A	XP_011526826.1:n.1545+98C>A
XM_017027625.2:c.1230+98C>A	XP_016883114.1:n.1230+98C>A
XM_024451822.1:c.1230+98C>A	XP_024307590.1:n.1230+98C>A
NM_001256573.2:c.1230+98C>A	NP_001243502.1:n.1230+98C>A
NR_046317.2:n.1967+98C>A
NM_000744.7:c.1758+98C>A MANE Select	NP_000735.1:n.1758+98C>A