Canonical Allele Identifier: CA511339032

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982256G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350904G>T , CM000682.2:g.63350904G>T	GRCh38
NC_000020.10:g.61982256G>T , CM000682.1:g.61982256G>T	GRCh37
NC_000020.9:g.61452700G>T	NCBI36
NG_011931.1:g.15440C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.507C>A MANE Select	ENSP00000359285.4:p.Pro169=
ENST00000370263.8:c.507C>A	ENSP00000359285.4:p.Pro169=
ENST00000463705.5:n.1155C>A
ENST00000467563.3:n.577C>A
ENST00000498043.6:c.531C>A
ENST00000615287.4:c.294C>A	ENSP00000483388.1:p.Pro98=
ENST00000627000.1:c.*196C>A	ENSP00000486914.1:n.*196C>A
ENST00000630240.1:n.228C>A
NM_000744.6:c.507C>A	NP_000735.1:p.Pro169=
NM_001256573.1:c.-22C>A	NP_001243502.1:n.-22C>A
NR_046317.1:n.763C>A
XM_011528524.1:c.294C>A	XP_011526826.1:p.Pro98=
XM_017027625.2:c.-22C>A	XP_016883114.1:n.-22C>A
XM_024451822.1:c.-22C>A	XP_024307590.1:n.-22C>A
NM_001256573.2:c.-22C>A	NP_001243502.1:n.-22C>A
NR_046317.2:n.716C>A
NM_000744.7:c.507C>A MANE Select	NP_000735.1:p.Pro169=