Canonical Allele Identifier: CA409632909

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981196G>A (hg19) ; chr20:g.63349844G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349844G>A , CM000682.2:g.63349844G>A	GRCh38
NC_000020.10:g.61981196G>A , CM000682.1:g.61981196G>A	GRCh37
NC_000020.9:g.61451640G>A	NCBI36
NG_011931.1:g.16500C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1567C>T MANE Select	ENSP00000359285.4:p.Pro523Ser
ENST00000370263.8:c.1567C>T	ENSP00000359285.4:p.Pro523Ser
ENST00000463705.5:n.2215C>T
ENST00000467563.3:n.1637C>T
ENST00000498043.6:c.1591C>T
ENST00000615287.4:c.1354C>T	ENSP00000483388.1:p.Pro452Ser
ENST00000627000.1:c.*1256C>T	ENSP00000486914.1:n.*1256C>T
ENST00000630240.1:n.1288C>T
NM_000744.6:c.1567C>T	NP_000735.1:p.Pro523Ser
NM_001256573.1:c.1039C>T	NP_001243502.1:p.Pro347Ser
NR_046317.1:n.1823C>T
XM_011528524.1:c.1354C>T	XP_011526826.1:p.Pro452Ser
XM_017027625.2:c.1039C>T	XP_016883114.1:p.Pro347Ser
XM_024451822.1:c.1039C>T	XP_024307590.1:p.Pro347Ser
NM_001256573.2:c.1039C>T	NP_001243502.1:p.Pro347Ser
NR_046317.2:n.1776C>T
NM_000744.7:c.1567C>T MANE Select	NP_000735.1:p.Pro523Ser