Canonical Allele Identifier: CA511338930

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981962C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350610C>A , CM000682.2:g.63350610C>A	GRCh38
NC_000020.10:g.61981962C>A , CM000682.1:g.61981962C>A	GRCh37
NC_000020.9:g.61452406C>A	NCBI36
NG_011931.1:g.15734G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.801G>T MANE Select	ENSP00000359285.4:p.Leu267=
ENST00000370263.8:c.801G>T	ENSP00000359285.4:p.Leu267=
ENST00000463705.5:n.1449G>T
ENST00000467563.3:n.871G>T
ENST00000498043.6:c.825G>T
ENST00000615287.4:c.588G>T	ENSP00000483388.1:p.Leu196=
ENST00000627000.1:c.*490G>T	ENSP00000486914.1:n.*490G>T
ENST00000630240.1:n.522G>T
NM_000744.6:c.801G>T	NP_000735.1:p.Leu267=
NM_001256573.1:c.273G>T	NP_001243502.1:p.Leu91=
NR_046317.1:n.1057G>T
XM_011528524.1:c.588G>T	XP_011526826.1:p.Leu196=
XM_017027625.2:c.273G>T	XP_016883114.1:p.Leu91=
XM_024451822.1:c.273G>T	XP_024307590.1:p.Leu91=
NM_001256573.2:c.273G>T	NP_001243502.1:p.Leu91=
NR_046317.2:n.1010G>T
NM_000744.7:c.801G>T MANE Select	NP_000735.1:p.Leu267=