Canonical Allele Identifier: CA1561548585

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87363618_87363619delinsAC , CM000667.2:g.87363618_87363619delinsAC GRCh38
NC_000005.9:g.86659435_86659436delinsAC , CM000667.1:g.86659435_86659436delinsAC GRCh37
NC_000005.8:g.86695191_86695192delinsAC NCBI36
NG_011650.1:g.100285_100286delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.1610+114_1610+115delinsAC (RASA1) MANE Select ENSP00000274376.6:n.1610+114_1610+115delinsAC
ENST00000645953.1:c.*90+29151_*90+29152delinsGT (CCNH) ENSP00000494460.1:n.*90+29151_*90+29152delinsGT
ENST00000274376.10:c.1610+114_1610+115delinsAC (RASA1) ENSP00000274376.6:n.1610+114_1610+115delinsAC
ENST00000456692.6:c.1079+114_1079+115delinsAC (RASA1) ENSP00000411221.2:n.1079+114_1079+115delinsAC
ENST00000506290.1:c.1112+114_1112+115delinsAC (RASA1) ENSP00000420905.1:n.1112+114_1112+115delinsAC
ENST00000509953.1:n.713+114_713+115delinsAC (RASA1)
ENST00000512763.5:c.1109+114_1109+115delinsAC (RASA1) ENSP00000422008.1:n.1109+114_1109+115delinsAC
ENST00000515800.6:c.1610+114_1610+115delinsAC (RASA1) ENSP00000423395.2:n.1610+114_1610+115delinsAC
NM_002890.2:c.1610+114_1610+115delinsAC (RASA1) NP_002881.1:n.1610+114_1610+115delinsAC
NM_022650.2:c.1079+114_1079+115delinsAC (RASA1) NP_072179.1:n.1079+114_1079+115delinsAC
XM_011543525.1:c.1610+114_1610+115delinsAC (RASA1) XP_011541827.1:n.1610+114_1610+115delinsAC
XM_011543526.1:c.1610+114_1610+115delinsAC (RASA1) XP_011541828.1:n.1610+114_1610+115delinsAC
XM_011543527.1:c.1610+114_1610+115delinsAC (RASA1) XP_011541829.1:n.1610+114_1610+115delinsAC
NM_001364075.1:c.933+31425_933+31426delinsGT (CCNH) NP_001351004.1:n.933+31425_933+31426delinsGT
NR_157068.1:n.1447+29151_1447+29152delinsGT (CCNH)
NR_157069.1:n.1040+29151_1040+29152delinsGT (CCNH)
NR_157070.1:n.1204+29151_1204+29152delinsGT (CCNH)
XM_011543525.2:c.1610+114_1610+115delinsAC (RASA1) XP_011541827.1:n.1610+114_1610+115delinsAC
XM_011543527.3:c.1610+114_1610+115delinsAC (RASA1) XP_011541829.1:n.1610+114_1610+115delinsAC
NM_001364075.2:c.933+31425_933+31426delinsGT (CCNH) NP_001351004.1:n.933+31425_933+31426delinsGT
NM_002890.3:c.1610+114_1610+115delinsAC (RASA1) MANE Select NP_002881.1:n.1610+114_1610+115delinsAC
NR_157068.2:n.1447+29151_1447+29152delinsGT (CCNH)
NR_157069.2:n.1040+29151_1040+29152delinsGT (CCNH)
NR_157070.2:n.1204+29151_1204+29152delinsGT (CCNH)
NM_022650.3:c.1079+114_1079+115delinsAC (RASA1) NP_072179.1:n.1079+114_1079+115delinsAC