Canonical Allele Identifier: CA511338972

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981896C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350544C>A , CM000682.2:g.63350544C>A	GRCh38
NC_000020.10:g.61981896C>A , CM000682.1:g.61981896C>A	GRCh37
NC_000020.9:g.61452340C>A	NCBI36
NG_011931.1:g.15800G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.867G>T MANE Select	ENSP00000359285.4:p.Leu289=
ENST00000370263.8:c.867G>T	ENSP00000359285.4:p.Leu289=
ENST00000463705.5:n.1515G>T
ENST00000467563.3:n.937G>T
ENST00000498043.6:c.891G>T
ENST00000615287.4:c.654G>T	ENSP00000483388.1:p.Leu218=
ENST00000627000.1:c.*556G>T	ENSP00000486914.1:n.*556G>T
ENST00000630240.1:n.588G>T
NM_000744.6:c.867G>T	NP_000735.1:p.Leu289=
NM_001256573.1:c.339G>T	NP_001243502.1:p.Leu113=
NR_046317.1:n.1123G>T
XM_011528524.1:c.654G>T	XP_011526826.1:p.Leu218=
XM_017027625.2:c.339G>T	XP_016883114.1:p.Leu113=
XM_024451822.1:c.339G>T	XP_024307590.1:p.Leu113=
NM_001256573.2:c.339G>T	NP_001243502.1:p.Leu113=
NR_046317.2:n.1076G>T
NM_000744.7:c.867G>T MANE Select	NP_000735.1:p.Leu289=