Canonical Allele Identifier: CA409635745

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981774A>C (hg19) ; chr20:g.63350422A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350422A>C , CM000682.2:g.63350422A>C	GRCh38
NC_000020.10:g.61981774A>C , CM000682.1:g.61981774A>C	GRCh37
NC_000020.9:g.61452218A>C	NCBI36
NG_011931.1:g.15922T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.989T>G MANE Select	ENSP00000359285.4:p.Val330Gly
ENST00000370263.8:c.989T>G	ENSP00000359285.4:p.Val330Gly
ENST00000463705.5:n.1637T>G
ENST00000467563.3:n.1059T>G
ENST00000498043.6:c.1013T>G
ENST00000615287.4:c.776T>G	ENSP00000483388.1:p.Val259Gly
ENST00000627000.1:c.*678T>G	ENSP00000486914.1:n.*678T>G
ENST00000630240.1:n.710T>G
NM_000744.6:c.989T>G	NP_000735.1:p.Val330Gly
NM_001256573.1:c.461T>G	NP_001243502.1:p.Val154Gly
NR_046317.1:n.1245T>G
XM_011528524.1:c.776T>G	XP_011526826.1:p.Val259Gly
XM_017027625.2:c.461T>G	XP_016883114.1:p.Val154Gly
XM_024451822.1:c.461T>G	XP_024307590.1:p.Val154Gly
NM_001256573.2:c.461T>G	NP_001243502.1:p.Val154Gly
NR_046317.2:n.1198T>G
NM_000744.7:c.989T>G MANE Select	NP_000735.1:p.Val330Gly