Canonical Allele Identifier: CA409638282

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350905-G-T
• MyVariant Identifiers: chr20:g.61982257G>T (hg19) ; chr20:g.63350905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350905G>T , CM000682.2:g.63350905G>T	GRCh38
NC_000020.10:g.61982257G>T , CM000682.1:g.61982257G>T	GRCh37
NC_000020.9:g.61452701G>T	NCBI36
NG_011931.1:g.15439C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.506C>A MANE Select	ENSP00000359285.4:p.Pro169His
ENST00000370263.8:c.506C>A	ENSP00000359285.4:p.Pro169His
ENST00000463705.5:n.1154C>A
ENST00000467563.3:n.576C>A
ENST00000498043.6:c.530C>A
ENST00000615287.4:c.293C>A	ENSP00000483388.1:p.Pro98His
ENST00000627000.1:c.*195C>A	ENSP00000486914.1:n.*195C>A
ENST00000630240.1:n.227C>A
NM_000744.6:c.506C>A	NP_000735.1:p.Pro169His
NM_001256573.1:c.-23C>A	NP_001243502.1:n.-23C>A
NR_046317.1:n.762C>A
XM_011528524.1:c.293C>A	XP_011526826.1:p.Pro98His
XM_017027625.2:c.-23C>A	XP_016883114.1:n.-23C>A
XM_024451822.1:c.-23C>A	XP_024307590.1:n.-23C>A
NM_001256573.2:c.-23C>A	NP_001243502.1:n.-23C>A
NR_046317.2:n.715C>A
NM_000744.7:c.506C>A MANE Select	NP_000735.1:p.Pro169His