Canonical Allele Identifier: CA409636752

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981979C>A (hg19) ; chr20:g.63350627C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350627C>A , CM000682.2:g.63350627C>A	GRCh38
NC_000020.10:g.61981979C>A , CM000682.1:g.61981979C>A	GRCh37
NC_000020.9:g.61452423C>A	NCBI36
NG_011931.1:g.15717G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.784G>T MANE Select	ENSP00000359285.4:p.Val262Leu
ENST00000370263.8:c.784G>T	ENSP00000359285.4:p.Val262Leu
ENST00000463705.5:n.1432G>T
ENST00000467563.3:n.854G>T
ENST00000498043.6:c.808G>T
ENST00000615287.4:c.571G>T	ENSP00000483388.1:p.Val191Leu
ENST00000627000.1:c.*473G>T	ENSP00000486914.1:n.*473G>T
ENST00000630240.1:n.505G>T
NM_000744.6:c.784G>T	NP_000735.1:p.Val262Leu
NM_001256573.1:c.256G>T	NP_001243502.1:p.Val86Leu
NR_046317.1:n.1040G>T
XM_011528524.1:c.571G>T	XP_011526826.1:p.Val191Leu
XM_017027625.2:c.256G>T	XP_016883114.1:p.Val86Leu
XM_024451822.1:c.256G>T	XP_024307590.1:p.Val86Leu
NM_001256573.2:c.256G>T	NP_001243502.1:p.Val86Leu
NR_046317.2:n.993G>T
NM_000744.7:c.784G>T MANE Select	NP_000735.1:p.Val262Leu