Canonical Allele Identifier: CA409636402

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350537-T-A
• MyVariant Identifiers: chr20:g.61981889T>A (hg19) ; chr20:g.63350537T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350537T>A , CM000682.2:g.63350537T>A	GRCh38
NC_000020.10:g.61981889T>A , CM000682.1:g.61981889T>A	GRCh37
NC_000020.9:g.61452333T>A	NCBI36
NG_011931.1:g.15807A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.874A>T MANE Select	ENSP00000359285.4:p.Ile292Phe
ENST00000370263.8:c.874A>T	ENSP00000359285.4:p.Ile292Phe
ENST00000463705.5:n.1522A>T
ENST00000467563.3:n.944A>T
ENST00000498043.6:c.898A>T
ENST00000615287.4:c.661A>T	ENSP00000483388.1:p.Ile221Phe
ENST00000627000.1:c.*563A>T	ENSP00000486914.1:n.*563A>T
ENST00000630240.1:n.595A>T
NM_000744.6:c.874A>T	NP_000735.1:p.Ile292Phe
NM_001256573.1:c.346A>T	NP_001243502.1:p.Ile116Phe
NR_046317.1:n.1130A>T
XM_011528524.1:c.661A>T	XP_011526826.1:p.Ile221Phe
XM_017027625.2:c.346A>T	XP_016883114.1:p.Ile116Phe
XM_024451822.1:c.346A>T	XP_024307590.1:p.Ile116Phe
NM_001256573.2:c.346A>T	NP_001243502.1:p.Ile116Phe
NR_046317.2:n.1083A>T
NM_000744.7:c.874A>T MANE Select	NP_000735.1:p.Ile292Phe