Canonical Allele Identifier: CA2577388996
Gene: SAMHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.36930870_36930885del , CM000682.2:g.36930870_36930885del GRCh38
NC_000020.10:g.35559273_35559288del , CM000682.1:g.35559273_35559288del GRCh37
NC_000020.9:g.34992687_34992702del NCBI36
NG_017059.1:g.25959_25974del , LRG_281:g.25959_25974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644114.2:c.510-10_515del
ENST00000644250.2:c.510-10_515del
ENST00000644688.2:n.572-10_577del
ENST00000645444.2:c.510-10_515del
ENST00000682773.1:c.510-10_515del
ENST00000683720.1:c.510-10_515del
ENST00000683766.1:c.510-10_515del
ENST00000262878.5:c.510-10_515del
ENST00000642186.1:c.510-10_515del
ENST00000642246.1:c.*189-10_*194del
ENST00000642616.1:c.458-10_463del
ENST00000643078.1:c.*189-10_*194del
ENST00000643161.1:n.73-10_78del
ENST00000643918.1:c.510-10_515del
ENST00000644114.1:c.436-10_441del
ENST00000644370.1:n.451-10_456del
ENST00000645033.1:c.510-10_515del
ENST00000645444.1:c.278-10_283del
ENST00000646066.1:c.510-10_515del
ENST00000646121.1:c.227-10_232del
ENST00000646673.2:c.510-10_515del
ENST00000646866.1:c.349-10_354del
ENST00000646869.1:c.510-10_515del
ENST00000646904.1:c.510-10_515del
ENST00000647095.1:n.581-10_586del
ENST00000647163.1:c.510-10_515del
ENST00000647459.1:n.537-10_542del
ENST00000262878.4:c.510-10_515del
NM_015474.3:c.510-10_515del , LRG_281t1:c.510-10_515del
XM_005260384.2:c.510-10_515del
XM_011528761.1:c.510-10_515del
NM_001363729.1:c.510-10_515del
NM_001363733.1:c.510-10_515del
NM_001363729.2:c.510-10_515del
NM_001363733.2:c.510-10_515del
NM_015474.4:c.510-10_515del