Canonical Allele Identifier: CA511338437

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981185G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349833G>A , CM000682.2:g.63349833G>A	GRCh38
NC_000020.10:g.61981185G>A , CM000682.1:g.61981185G>A	GRCh37
NC_000020.9:g.61451629G>A	NCBI36
NG_011931.1:g.16511C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1578C>T MANE Select	ENSP00000359285.4:p.Pro526=
ENST00000370263.8:c.1578C>T	ENSP00000359285.4:p.Pro526=
ENST00000463705.5:n.2226C>T
ENST00000467563.3:n.1648C>T
ENST00000498043.6:c.1602C>T
ENST00000615287.4:c.1365C>T	ENSP00000483388.1:p.Pro455=
ENST00000627000.1:c.*1267C>T	ENSP00000486914.1:n.*1267C>T
ENST00000630240.1:n.1299C>T
NM_000744.6:c.1578C>T	NP_000735.1:p.Pro526=
NM_001256573.1:c.1050C>T	NP_001243502.1:p.Pro350=
NR_046317.1:n.1834C>T
XM_011528524.1:c.1365C>T	XP_011526826.1:p.Pro455=
XM_017027625.2:c.1050C>T	XP_016883114.1:p.Pro350=
XM_024451822.1:c.1050C>T	XP_024307590.1:p.Pro350=
NM_001256573.2:c.1050C>T	NP_001243502.1:p.Pro350=
NR_046317.2:n.1787C>T
NM_000744.7:c.1578C>T MANE Select	NP_000735.1:p.Pro526=