Canonical Allele Identifier: CA409635351

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981708A>C (hg19) ; chr20:g.63350356A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350356A>C , CM000682.2:g.63350356A>C	GRCh38
NC_000020.10:g.61981708A>C , CM000682.1:g.61981708A>C	GRCh37
NC_000020.9:g.61452152A>C	NCBI36
NG_011931.1:g.15988T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1055T>G MANE Select	ENSP00000359285.4:p.Val352Gly
ENST00000370263.8:c.1055T>G	ENSP00000359285.4:p.Val352Gly
ENST00000463705.5:n.1703T>G
ENST00000467563.3:n.1125T>G
ENST00000498043.6:c.1079T>G
ENST00000615287.4:c.842T>G	ENSP00000483388.1:p.Val281Gly
ENST00000627000.1:c.*744T>G	ENSP00000486914.1:n.*744T>G
ENST00000630240.1:n.776T>G
NM_000744.6:c.1055T>G	NP_000735.1:p.Val352Gly
NM_001256573.1:c.527T>G	NP_001243502.1:p.Val176Gly
NR_046317.1:n.1311T>G
XM_011528524.1:c.842T>G	XP_011526826.1:p.Val281Gly
XM_017027625.2:c.527T>G	XP_016883114.1:p.Val176Gly
XM_024451822.1:c.527T>G	XP_024307590.1:p.Val176Gly
NM_001256573.2:c.527T>G	NP_001243502.1:p.Val176Gly
NR_046317.2:n.1264T>G
NM_000744.7:c.1055T>G MANE Select	NP_000735.1:p.Val352Gly