Canonical Allele Identifier: CA1139658946

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87338008_87338012del , CM000667.2:g.87338008_87338012del GRCh38
NC_000005.9:g.86633825_86633829del , CM000667.1:g.86633825_86633829del GRCh37
NC_000005.8:g.86669581_86669585del NCBI36
NG_011650.1:g.74675_74679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.934_938del (RASA1) MANE Select ENSP00000274376.6:p.Glu312ArgfsTer14
ENST00000645953.1:c.*91-19114_*91-19110del (CCNH) ENSP00000494460.1:n.*91-19114_*91-19110del
ENST00000274376.10:c.934_938del (RASA1) ENSP00000274376.6:p.Glu312ArgfsTer14
ENST00000456692.6:c.403_407del (RASA1) ENSP00000411221.2:p.Glu135ArgfsTer14
ENST00000506290.1:c.436_440del (RASA1) ENSP00000420905.1:p.Glu146ArgfsTer14
ENST00000509953.1:n.37_41del (RASA1)
ENST00000512763.5:c.433_437del (RASA1) ENSP00000422008.1:p.Glu145ArgfsTer14
ENST00000515800.6:c.934_938del (RASA1) ENSP00000423395.2:p.Glu312ArgfsTer14
NM_002890.2:c.934_938del (RASA1) NP_002881.1:p.Glu312ArgfsTer14
NM_022650.2:c.403_407del (RASA1) NP_072179.1:p.Glu135ArgfsTer14
XM_011543525.1:c.934_938del (RASA1) XP_011541827.1:p.Glu312ArgfsTer14
XM_011543526.1:c.934_938del (RASA1) XP_011541828.1:p.Glu312ArgfsTer14
XM_011543527.1:c.934_938del (RASA1) XP_011541829.1:p.Glu312ArgfsTer14
NM_001364075.1:c.934-25216_934-25212del (CCNH) NP_001351004.1:n.934-25216_934-25212del
NR_157068.1:n.1448-25216_1448-25212del (CCNH)
NR_157069.1:n.1041-25216_1041-25212del (CCNH)
NR_157070.1:n.1205-25216_1205-25212del (CCNH)
XM_011543525.2:c.934_938del (RASA1) XP_011541827.1:p.Glu312ArgfsTer14
XM_011543527.3:c.934_938del (RASA1) XP_011541829.1:p.Glu312ArgfsTer14
NM_001364075.2:c.934-25216_934-25212del (CCNH) NP_001351004.1:n.934-25216_934-25212del
NM_002890.3:c.934_938del (RASA1) MANE Select NP_002881.1:p.Glu312ArgfsTer14
NR_157068.2:n.1448-25216_1448-25212del (CCNH)
NR_157069.2:n.1041-25216_1041-25212del (CCNH)
NR_157070.2:n.1205-25216_1205-25212del (CCNH)
NM_022650.3:c.403_407del (RASA1) NP_072179.1:p.Glu135ArgfsTer14