Canonical Allele Identifier: CA511204287

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981125G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349773G>A , CM000682.2:g.63349773G>A	GRCh38
NC_000020.10:g.61981125G>A , CM000682.1:g.61981125G>A	GRCh37
NC_000020.9:g.61451569G>A	NCBI36
NG_011931.1:g.16571C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.1638C>T MANE Select	ENSP00000359285.4:p.Val546=
ENST00000370263.8:c.1638C>T	ENSP00000359285.4:p.Val546=
ENST00000463705.5:n.2286C>T
ENST00000467563.3:n.1708C>T
ENST00000498043.6:c.1662C>T
ENST00000615287.4:c.1425C>T	ENSP00000483388.1:p.Val475=
ENST00000627000.1:c.*1327C>T	ENSP00000486914.1:n.*1327C>T
ENST00000630240.1:n.1359C>T
NM_000744.6:c.1638C>T	NP_000735.1:p.Val546=
NM_001256573.1:c.1110C>T	NP_001243502.1:p.Val370=
NR_046317.1:n.1894C>T
XM_011528524.1:c.1425C>T	XP_011526826.1:p.Val475=
XM_017027625.2:c.1110C>T	XP_016883114.1:p.Val370=
XM_024451822.1:c.1110C>T	XP_024307590.1:p.Val370=
NM_001256573.2:c.1110C>T	NP_001243502.1:p.Val370=
NR_046317.2:n.1847C>T
NM_000744.7:c.1638C>T MANE Select	NP_000735.1:p.Val546=