Canonical Allele Identifier: CA409636864

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982007G>C (hg19) ; chr20:g.63350655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350655G>C , CM000682.2:g.63350655G>C	GRCh38
NC_000020.10:g.61982007G>C , CM000682.1:g.61982007G>C	GRCh37
NC_000020.9:g.61452451G>C	NCBI36
NG_011931.1:g.15689C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.756C>G MANE Select	ENSP00000359285.4:p.Ile252Met
ENST00000370263.8:c.756C>G	ENSP00000359285.4:p.Ile252Met
ENST00000463705.5:n.1404C>G
ENST00000467563.3:n.826C>G
ENST00000498043.6:c.780C>G
ENST00000615287.4:c.543C>G	ENSP00000483388.1:p.Ile181Met
ENST00000627000.1:c.*445C>G	ENSP00000486914.1:n.*445C>G
ENST00000630240.1:n.477C>G
NM_000744.6:c.756C>G	NP_000735.1:p.Ile252Met
NM_001256573.1:c.228C>G	NP_001243502.1:p.Ile76Met
NR_046317.1:n.1012C>G
XM_011528524.1:c.543C>G	XP_011526826.1:p.Ile181Met
XM_017027625.2:c.228C>G	XP_016883114.1:p.Ile76Met
XM_024451822.1:c.228C>G	XP_024307590.1:p.Ile76Met
NM_001256573.2:c.228C>G	NP_001243502.1:p.Ile76Met
NR_046317.2:n.965C>G
NM_000744.7:c.756C>G MANE Select	NP_000735.1:p.Ile252Met