Canonical Allele Identifier: CA511339158

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982160C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350808C>G , CM000682.2:g.63350808C>G	GRCh38
NC_000020.10:g.61982160C>G , CM000682.1:g.61982160C>G	GRCh37
NC_000020.9:g.61452604C>G	NCBI36
NG_011931.1:g.15536G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.603G>C MANE Select	ENSP00000359285.4:p.Leu201=
ENST00000370263.8:c.603G>C	ENSP00000359285.4:p.Leu201=
ENST00000463705.5:n.1251G>C
ENST00000467563.3:n.673G>C
ENST00000498043.6:c.627G>C
ENST00000615287.4:c.390G>C	ENSP00000483388.1:p.Leu130=
ENST00000627000.1:c.*292G>C	ENSP00000486914.1:n.*292G>C
ENST00000630240.1:n.324G>C
NM_000744.6:c.603G>C	NP_000735.1:p.Leu201=
NM_001256573.1:c.75G>C	NP_001243502.1:p.Leu25=
NR_046317.1:n.859G>C
XM_011528524.1:c.390G>C	XP_011526826.1:p.Leu130=
XM_017027625.2:c.75G>C	XP_016883114.1:p.Leu25=
XM_024451822.1:c.75G>C	XP_024307590.1:p.Leu25=
NM_001256573.2:c.75G>C	NP_001243502.1:p.Leu25=
NR_046317.2:n.812G>C
NM_000744.7:c.603G>C MANE Select	NP_000735.1:p.Leu201=