Canonical Allele Identifier: CA409638127

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982233A>T (hg19) ; chr20:g.63350881A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350881A>T , CM000682.2:g.63350881A>T	GRCh38
NC_000020.10:g.61982233A>T , CM000682.1:g.61982233A>T	GRCh37
NC_000020.9:g.61452677A>T	NCBI36
NG_011931.1:g.15463T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.530T>A MANE Select	ENSP00000359285.4:p.Met177Lys
ENST00000370263.8:c.530T>A	ENSP00000359285.4:p.Met177Lys
ENST00000463705.5:n.1178T>A
ENST00000467563.3:n.600T>A
ENST00000498043.6:c.554T>A
ENST00000615287.4:c.317T>A	ENSP00000483388.1:p.Met106Lys
ENST00000627000.1:c.*219T>A	ENSP00000486914.1:n.*219T>A
ENST00000630240.1:n.251T>A
NM_000744.6:c.530T>A	NP_000735.1:p.Met177Lys
NM_001256573.1:c.2T>A	NP_001243502.1:p.Met1Lys
NR_046317.1:n.786T>A
XM_011528524.1:c.317T>A	XP_011526826.1:p.Met106Lys
XM_017027625.2:c.2T>A	XP_016883114.1:p.Met1Lys
XM_024451822.1:c.2T>A	XP_024307590.1:p.Met1Lys
NM_001256573.2:c.2T>A	NP_001243502.1:p.Met1Lys
NR_046317.2:n.739T>A
NM_000744.7:c.530T>A MANE Select	NP_000735.1:p.Met177Lys