Canonical Allele Identifier: CA2577388747

Gene: SAMHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.36904260C>T , CM000682.2:g.36904260C>T	GRCh38
NC_000020.10:g.35532663C>T , CM000682.1:g.35532663C>T	GRCh37
NC_000020.9:g.34966077C>T	NCBI36
NG_017059.1:g.52584G>A , LRG_281:g.52584G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644114.2:c.1271-5716G>A	ENSP00000494354.2:n.1271-5716G>A
ENST00000644250.2:c.1411-11G>A	ENSP00000493810.2:n.1411-11G>A
ENST00000644688.2:n.1473-11G>A
ENST00000645444.2:c.*2818G>A	ENSP00000495381.2:n.*2818G>A
ENST00000682773.1:c.1411-11G>A	ENSP00000507178.1:n.1411-11G>A
ENST00000683720.1:c.1449-11G>A	ENSP00000508219.1:n.1449-11G>A
ENST00000683766.1:c.1411-11G>A	ENSP00000506877.1:n.1411-11G>A
ENST00000262878.5:c.1411-11G>A	ENSP00000262878.5:n.1411-11G>A
ENST00000465985.2:c.32-11G>A
ENST00000642186.1:c.*1715-11G>A	ENSP00000494436.1:n.*1715-11G>A
ENST00000642246.1:c.*1090-11G>A	ENSP00000494979.1:n.*1090-11G>A
ENST00000643825.1:c.34-11G>A	ENSP00000495448.1:n.34-11G>A
ENST00000643918.1:c.1411-11G>A	ENSP00000493928.1:n.1411-11G>A
ENST00000644114.1:c.1197-5716G>A
ENST00000644688.1:n.724-11G>A
ENST00000645033.1:c.*588-11G>A	ENSP00000494520.1:n.*588-11G>A
ENST00000645444.1:c.3456G>A
ENST00000646066.1:c.1201-11G>A	ENSP00000495432.1:n.1201-11G>A
ENST00000646673.2:c.1411-11G>A MANE Select	ENSP00000493536.2:n.1411-11G>A
ENST00000646869.1:c.1411-11G>A	ENSP00000495667.1:n.1411-11G>A
ENST00000646904.1:c.*617-11G>A	ENSP00000494823.1:n.*617-11G>A
ENST00000647095.1:n.2609-11G>A
ENST00000647163.1:c.*588-11G>A	ENSP00000494313.1:n.*588-11G>A
ENST00000647459.1:n.2565-11G>A
ENST00000262878.4:c.1411-11G>A	ENSP00000262878.4:n.1411-11G>A
ENST00000465985.1:n.32-11G>A
NM_015474.3:c.1411-11G>A , LRG_281t1:c.1411-11G>A	NP_056289.2:n.1411-11G>A
XM_005260384.2:c.1411-11G>A	XP_005260441.1:n.1411-11G>A
XM_011528761.1:c.1411-11G>A	XP_011527063.1:n.1411-11G>A
NM_001363729.1:c.1411-11G>A	NP_001350658.1:n.1411-11G>A
NM_001363733.1:c.1411-11G>A	NP_001350662.1:n.1411-11G>A
NM_001363729.2:c.1411-11G>A	NP_001350658.1:n.1411-11G>A
NM_001363733.2:c.1411-11G>A	NP_001350662.1:n.1411-11G>A
NM_015474.4:c.1411-11G>A MANE Select	NP_056289.2:n.1411-11G>A