Canonical Allele Identifier: CA313524

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 205002
• ClinVar RCV Id: RCV000186911 ; RCV000726687 ; RCV001085092 ; RCV002399695
• dbSNP Id: rs142646795
• ExAC: 20:61981203 G / A
• gnomAD v2: 20-61981203-G-A
• gnomAD v3: 20-63349851-G-A
• gnomAD v4: 20-63349851-G-A
• MyVariant Identifiers: chr20:g.61981203G>A (hg19) ; chr20:g.63349851G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349851G>A , CM000682.2:g.63349851G>A	GRCh38
NC_000020.10:g.61981203G>A , CM000682.1:g.61981203G>A	GRCh37
NC_000020.9:g.61451647G>A	NCBI36
NG_011931.1:g.16493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1560C>T MANE Select	ENSP00000359285.4:p.Leu520=
ENST00000370263.8:c.1560C>T	ENSP00000359285.4:p.Leu520=
ENST00000463705.5:n.2208C>T
ENST00000467563.3:n.1630C>T
ENST00000498043.6:c.1584C>T
ENST00000615287.4:c.1347C>T	ENSP00000483388.1:p.Leu449=
ENST00000627000.1:c.*1249C>T	ENSP00000486914.1:n.*1249C>T
ENST00000630240.1:n.1281C>T
NM_000744.6:c.1560C>T	NP_000735.1:p.Leu520=
NM_001256573.1:c.1032C>T	NP_001243502.1:p.Leu344=
NR_046317.1:n.1816C>T
XM_011528524.1:c.1347C>T	XP_011526826.1:p.Leu449=
XM_017027625.2:c.1032C>T	XP_016883114.1:p.Leu344=
XM_024451822.1:c.1032C>T	XP_024307590.1:p.Leu344=
NM_001256573.2:c.1032C>T	NP_001243502.1:p.Leu344=
NR_046317.2:n.1769C>T
NM_000744.7:c.1560C>T MANE Select	NP_000735.1:p.Leu520=