Canonical Allele Identifier: CA2362322128
Gene: SAMHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.36935000G= , CM000682.2:g.36935000G= GRCh38
NC_000020.10:g.35563403G= , CM000682.1:g.35563403G= GRCh37
NC_000020.9:g.34996817G= NCBI36
NG_017059.1:g.21844C= , LRG_281:g.21844C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644114.2:c.509+29C= ENSP00000494354.2:n.509+29C=
ENST00000644250.2:c.509+29C= ENSP00000493810.2:n.509+29C=
ENST00000644688.2:n.571+29C=
ENST00000645444.2:c.509+29C= ENSP00000495381.2:n.509+29C=
ENST00000682773.1:c.509+29C= ENSP00000507178.1:n.509+29C=
ENST00000683720.1:c.509+29C= ENSP00000508219.1:n.509+29C=
ENST00000683766.1:c.509+29C= ENSP00000506877.1:n.509+29C=
ENST00000262878.5:c.509+29C= ENSP00000262878.5:n.509+29C=
ENST00000642186.1:c.509+29C= ENSP00000494436.1:n.509+29C=
ENST00000642246.1:c.*188+29C= ENSP00000494979.1:n.*188+29C=
ENST00000642616.1:c.457+81C= ENSP00000494271.1:n.457+81C=
ENST00000643003.1:n.204C=
ENST00000643078.1:c.*188+29C= ENSP00000496474.1:n.*188+29C=
ENST00000643918.1:c.509+29C= ENSP00000493928.1:n.509+29C=
ENST00000644114.1:c.435+29C=
ENST00000644370.1:n.450+29C=
ENST00000645033.1:c.509+29C= ENSP00000494520.1:n.509+29C=
ENST00000645444.1:c.277+29C=
ENST00000646066.1:c.509+29C= ENSP00000495432.1:n.509+29C=
ENST00000646121.1:c.227-4125C=
ENST00000646673.2:c.509+29C= MANE Select ENSP00000493536.2:n.509+29C=
ENST00000646866.1:c.349-4125C= ENSP00000495737.1:n.349-4125C=
ENST00000646869.1:c.509+29C= ENSP00000495667.1:n.509+29C=
ENST00000646904.1:c.509+29C= ENSP00000494823.1:n.509+29C=
ENST00000647095.1:n.580+29C=
ENST00000647163.1:c.509+29C= ENSP00000494313.1:n.509+29C=
ENST00000647459.1:n.536+29C=
ENST00000262878.4:c.509+29C= ENSP00000262878.4:n.509+29C=
NM_015474.3:c.509+29C= , LRG_281t1:c.509+29C= NP_056289.2:n.509+29C=
XM_005260384.2:c.509+29C= XP_005260441.1:n.509+29C=
XM_011528761.1:c.509+29C= XP_011527063.1:n.509+29C=
NM_001363729.1:c.509+29C= NP_001350658.1:n.509+29C=
NM_001363733.1:c.509+29C= NP_001350662.1:n.509+29C=
NM_001363729.2:c.509+29C= NP_001350658.1:n.509+29C=
NM_001363733.2:c.509+29C= NP_001350662.1:n.509+29C=
NM_015474.4:c.509+29C= MANE Select NP_056289.2:n.509+29C=