Canonical Allele Identifier: CA409635386

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981715C>T (hg19) ; chr20:g.63350363C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350363C>T , CM000682.2:g.63350363C>T	GRCh38
NC_000020.10:g.61981715C>T , CM000682.1:g.61981715C>T	GRCh37
NC_000020.9:g.61452159C>T	NCBI36
NG_011931.1:g.15981G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1048G>A MANE Select	ENSP00000359285.4:p.Asp350Asn
ENST00000370263.8:c.1048G>A	ENSP00000359285.4:p.Asp350Asn
ENST00000463705.5:n.1696G>A
ENST00000467563.3:n.1118G>A
ENST00000498043.6:c.1072G>A
ENST00000615287.4:c.835G>A	ENSP00000483388.1:p.Asp279Asn
ENST00000627000.1:c.*737G>A	ENSP00000486914.1:n.*737G>A
ENST00000630240.1:n.769G>A
NM_000744.6:c.1048G>A	NP_000735.1:p.Asp350Asn
NM_001256573.1:c.520G>A	NP_001243502.1:p.Asp174Asn
NR_046317.1:n.1304G>A
XM_011528524.1:c.835G>A	XP_011526826.1:p.Asp279Asn
XM_017027625.2:c.520G>A	XP_016883114.1:p.Asp174Asn
XM_024451822.1:c.520G>A	XP_024307590.1:p.Asp174Asn
NM_001256573.2:c.520G>A	NP_001243502.1:p.Asp174Asn
NR_046317.2:n.1257G>A
NM_000744.7:c.1048G>A MANE Select	NP_000735.1:p.Asp350Asn