Canonical Allele Identifier: CA2695204741

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331364_87331370del , CM000667.2:g.87331364_87331370del GRCh38
NC_000005.9:g.86627181_86627187del , CM000667.1:g.86627181_86627187del GRCh37
NC_000005.8:g.86662937_86662943del NCBI36
NG_011650.1:g.68031_68037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.556_562del (RASA1) MANE Select ENSP00000274376.6:p.Leu186GlufsTer3
ENST00000645953.1:c.*91-12472_*91-12466del (CCNH) ENSP00000494460.1:n.*91-12472_*91-12466del
ENST00000274376.10:c.556_562del (RASA1) ENSP00000274376.6:p.Leu186GlufsTer3
ENST00000456692.6:c.25_31del (RASA1) ENSP00000411221.2:p.Leu9GlufsTer3
ENST00000506290.1:c.58_64del (RASA1) ENSP00000420905.1:p.Leu20GlufsTer3
ENST00000512763.5:c.55_61del (RASA1) ENSP00000422008.1:p.Leu19GlufsTer3
ENST00000515800.6:c.556_562del (RASA1) ENSP00000423395.2:p.Leu186GlufsTer3
NM_002890.2:c.556_562del (RASA1) NP_002881.1:p.Leu186GlufsTer3
NM_022650.2:c.25_31del (RASA1) NP_072179.1:p.Leu9GlufsTer3
XM_011543525.1:c.556_562del (RASA1) XP_011541827.1:p.Leu186GlufsTer3
XM_011543526.1:c.556_562del (RASA1) XP_011541828.1:p.Leu186GlufsTer3
XM_011543527.1:c.556_562del (RASA1) XP_011541829.1:p.Leu186GlufsTer3
NM_001364075.1:c.934-18574_934-18568del (CCNH) NP_001351004.1:n.934-18574_934-18568del
NR_157068.1:n.1448-18574_1448-18568del (CCNH)
NR_157069.1:n.1041-18574_1041-18568del (CCNH)
NR_157070.1:n.1205-18574_1205-18568del (CCNH)
XM_011543525.2:c.556_562del (RASA1) XP_011541827.1:p.Leu186GlufsTer3
XM_011543527.3:c.556_562del (RASA1) XP_011541829.1:p.Leu186GlufsTer3
NM_001364075.2:c.934-18574_934-18568del (CCNH) NP_001351004.1:n.934-18574_934-18568del
NM_002890.3:c.556_562del (RASA1) MANE Select NP_002881.1:p.Leu186GlufsTer3
NR_157068.2:n.1448-18574_1448-18568del (CCNH)
NR_157069.2:n.1041-18574_1041-18568del (CCNH)
NR_157070.2:n.1205-18574_1205-18568del (CCNH)
NM_022650.3:c.25_31del (RASA1) NP_072179.1:p.Leu9GlufsTer3