Canonical Allele Identifier: CA303018

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 136757
• ClinVar RCV Id: RCV000178803 ; RCV000460929
• dbSNP Id: rs76270730
• ExAC: 20:61981785 G / A
• gnomAD v2: 20-61981785-G-A
• gnomAD v3: 20-63350433-G-A
• gnomAD v4: 20-63350433-G-A
• MyVariant Identifiers: chr20:g.61981785G>A (hg19) ; chr20:g.63350433G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350433G>A , CM000682.2:g.63350433G>A	GRCh38
NC_000020.10:g.61981785G>A , CM000682.1:g.61981785G>A	GRCh37
NC_000020.9:g.61452229G>A	NCBI36
NG_011931.1:g.15911C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.978C>T MANE Select	ENSP00000359285.4:p.Phe326=
ENST00000370263.8:c.978C>T	ENSP00000359285.4:p.Phe326=
ENST00000463705.5:n.1626C>T
ENST00000467563.3:n.1048C>T
ENST00000498043.6:c.1002C>T
ENST00000615287.4:c.765C>T	ENSP00000483388.1:p.Phe255=
ENST00000627000.1:c.*667C>T	ENSP00000486914.1:n.*667C>T
ENST00000630240.1:n.699C>T
NM_000744.6:c.978C>T	NP_000735.1:p.Phe326=
NM_001256573.1:c.450C>T	NP_001243502.1:p.Phe150=
NR_046317.1:n.1234C>T
XM_011528524.1:c.765C>T	XP_011526826.1:p.Phe255=
XM_017027625.2:c.450C>T	XP_016883114.1:p.Phe150=
XM_024451822.1:c.450C>T	XP_024307590.1:p.Phe150=
NM_001256573.2:c.450C>T	NP_001243502.1:p.Phe150=
NR_046317.2:n.1187C>T
NM_000744.7:c.978C>T MANE Select	NP_000735.1:p.Phe326=