Canonical Allele Identifier: CA2653788348

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63349559-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349559G>A , CM000682.2:g.63349559G>A	GRCh38
NC_000020.10:g.61980911G>A , CM000682.1:g.61980911G>A	GRCh37
NC_000020.9:g.61451355G>A	NCBI36
NG_011931.1:g.16785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1758+94C>T MANE Select	ENSP00000359285.4:n.1758+94C>T
ENST00000370263.8:c.1758+94C>T	ENSP00000359285.4:n.1758+94C>T
ENST00000463705.5:n.2406+94C>T
ENST00000467563.3:n.1828+94C>T
ENST00000498043.6:c.1782+94C>T
ENST00000615287.4:c.1545+94C>T	ENSP00000483388.1:n.1545+94C>T
ENST00000627000.1:c.*1447+94C>T	ENSP00000486914.1:n.*1447+94C>T
ENST00000630240.1:n.1573C>T
NM_000744.6:c.1758+94C>T	NP_000735.1:n.1758+94C>T
NM_001256573.1:c.1230+94C>T	NP_001243502.1:n.1230+94C>T
NR_046317.1:n.2014+94C>T
XM_011528524.1:c.1545+94C>T	XP_011526826.1:n.1545+94C>T
XM_017027625.2:c.1230+94C>T	XP_016883114.1:n.1230+94C>T
XM_024451822.1:c.1230+94C>T	XP_024307590.1:n.1230+94C>T
NM_001256573.2:c.1230+94C>T	NP_001243502.1:n.1230+94C>T
NR_046317.2:n.1967+94C>T
NM_000744.7:c.1758+94C>T MANE Select	NP_000735.1:n.1758+94C>T