Canonical Allele Identifier: CA511338750

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981773C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350421C>G , CM000682.2:g.63350421C>G	GRCh38
NC_000020.10:g.61981773C>G , CM000682.1:g.61981773C>G	GRCh37
NC_000020.9:g.61452217C>G	NCBI36
NG_011931.1:g.15923G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.990G>C MANE Select	ENSP00000359285.4:p.Val330=
ENST00000370263.8:c.990G>C	ENSP00000359285.4:p.Val330=
ENST00000463705.5:n.1638G>C
ENST00000467563.3:n.1060G>C
ENST00000498043.6:c.1014G>C
ENST00000615287.4:c.777G>C	ENSP00000483388.1:p.Val259=
ENST00000627000.1:c.*679G>C	ENSP00000486914.1:n.*679G>C
ENST00000630240.1:n.711G>C
NM_000744.6:c.990G>C	NP_000735.1:p.Val330=
NM_001256573.1:c.462G>C	NP_001243502.1:p.Val154=
NR_046317.1:n.1246G>C
XM_011528524.1:c.777G>C	XP_011526826.1:p.Val259=
XM_017027625.2:c.462G>C	XP_016883114.1:p.Val154=
XM_024451822.1:c.462G>C	XP_024307590.1:p.Val154=
NM_001256573.2:c.462G>C	NP_001243502.1:p.Val154=
NR_046317.2:n.1199G>C
NM_000744.7:c.990G>C MANE Select	NP_000735.1:p.Val330=