Canonical Allele Identifier: CA408822380

Gene: SAMHD1

Linked Data

• MyVariant Identifiers: chr20:g.35559273C>A (hg19) ; chr20:g.36930870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.36930870C>A , CM000682.2:g.36930870C>A	GRCh38
NC_000020.10:g.35559273C>A , CM000682.1:g.35559273C>A	GRCh37
NC_000020.9:g.34992687C>A	NCBI36
NG_017059.1:g.25974G>T , LRG_281:g.25974G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644114.2:c.515G>T	ENSP00000494354.2:p.Gly172Val
ENST00000644250.2:c.515G>T	ENSP00000493810.2:p.Gly172Val
ENST00000644688.2:n.577G>T
ENST00000645444.2:c.515G>T	ENSP00000495381.2:p.Gly172Val
ENST00000682773.1:c.515G>T	ENSP00000507178.1:p.Gly172Val
ENST00000683720.1:c.515G>T	ENSP00000508219.1:p.Gly172Val
ENST00000683766.1:c.515G>T	ENSP00000506877.1:p.Gly172Val
ENST00000262878.5:c.515G>T	ENSP00000262878.5:p.Gly172Val
ENST00000642186.1:c.515G>T	ENSP00000494436.1:p.Gly172Val
ENST00000642246.1:c.*194G>T	ENSP00000494979.1:n.*194G>T
ENST00000642616.1:c.463G>T	ENSP00000494271.1:p.Gly155Cys
ENST00000643078.1:c.*194G>T	ENSP00000496474.1:n.*194G>T
ENST00000643161.1:n.78G>T
ENST00000643918.1:c.515G>T	ENSP00000493928.1:p.Gly172Val
ENST00000644114.1:c.441G>T
ENST00000644370.1:n.456G>T
ENST00000645033.1:c.515G>T	ENSP00000494520.1:p.Gly172Val
ENST00000645444.1:c.283G>T
ENST00000646066.1:c.515G>T	ENSP00000495432.1:p.Gly172Val
ENST00000646121.1:c.232G>T
ENST00000646673.2:c.515G>T MANE Select	ENSP00000493536.2:p.Gly172Val
ENST00000646866.1:c.354G>T	ENSP00000495737.1:p.Gly118=
ENST00000646869.1:c.515G>T	ENSP00000495667.1:p.Gly172Val
ENST00000646904.1:c.515G>T	ENSP00000494823.1:p.Gly172Val
ENST00000647095.1:n.586G>T
ENST00000647163.1:c.515G>T	ENSP00000494313.1:p.Gly172Val
ENST00000647459.1:n.542G>T
ENST00000262878.4:c.515G>T	ENSP00000262878.4:p.Gly172Val
NM_015474.3:c.515G>T , LRG_281t1:c.515G>T	NP_056289.2:p.Gly172Val
XM_005260384.2:c.515G>T	XP_005260441.1:p.Gly172Val
XM_011528761.1:c.515G>T	XP_011527063.1:p.Gly172Val
NM_001363729.1:c.515G>T	NP_001350658.1:p.Gly172Val
NM_001363733.1:c.515G>T	NP_001350662.1:p.Gly172Val
NM_001363729.2:c.515G>T	NP_001350658.1:p.Gly172Val
NM_001363733.2:c.515G>T	NP_001350662.1:p.Gly172Val
NM_015474.4:c.515G>T MANE Select	NP_056289.2:p.Gly172Val