Canonical Allele Identifier: CA511338417

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981176G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349824G>A , CM000682.2:g.63349824G>A	GRCh38
NC_000020.10:g.61981176G>A , CM000682.1:g.61981176G>A	GRCh37
NC_000020.9:g.61451620G>A	NCBI36
NG_011931.1:g.16520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1587C>T MANE Select	ENSP00000359285.4:p.Cys529=
ENST00000370263.8:c.1587C>T	ENSP00000359285.4:p.Cys529=
ENST00000463705.5:n.2235C>T
ENST00000467563.3:n.1657C>T
ENST00000498043.6:c.1611C>T
ENST00000615287.4:c.1374C>T	ENSP00000483388.1:p.Cys458=
ENST00000627000.1:c.*1276C>T	ENSP00000486914.1:n.*1276C>T
ENST00000630240.1:n.1308C>T
NM_000744.6:c.1587C>T	NP_000735.1:p.Cys529=
NM_001256573.1:c.1059C>T	NP_001243502.1:p.Cys353=
NR_046317.1:n.1843C>T
XM_011528524.1:c.1374C>T	XP_011526826.1:p.Cys458=
XM_017027625.2:c.1059C>T	XP_016883114.1:p.Cys353=
XM_024451822.1:c.1059C>T	XP_024307590.1:p.Cys353=
NM_001256573.2:c.1059C>T	NP_001243502.1:p.Cys353=
NR_046317.2:n.1796C>T
NM_000744.7:c.1587C>T MANE Select	NP_000735.1:p.Cys529=