Canonical Allele Identifier: CA1561548662

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87363681_87363683delinsTCA , CM000667.2:g.87363681_87363683delinsTCA GRCh38
NC_000005.9:g.86659498_86659500delinsTCA , CM000667.1:g.86659498_86659500delinsTCA GRCh37
NC_000005.8:g.86695254_86695256delinsTCA NCBI36
NG_011650.1:g.100348_100350delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.1610+177_1610+179delinsTCA (RASA1) MANE Select ENSP00000274376.6:n.1610+177_1610+179delinsTCA
ENST00000645953.1:c.*90+29087_*90+29089delinsTGA (CCNH) ENSP00000494460.1:n.*90+29087_*90+29089delinsTGA
ENST00000274376.10:c.1610+177_1610+179delinsTCA (RASA1) ENSP00000274376.6:n.1610+177_1610+179delinsTCA
ENST00000456692.6:c.1079+177_1079+179delinsTCA (RASA1) ENSP00000411221.2:n.1079+177_1079+179delinsTCA
ENST00000506290.1:c.1112+177_1112+179delinsTCA (RASA1) ENSP00000420905.1:n.1112+177_1112+179delinsTCA
ENST00000509953.1:n.713+177_713+179delinsTCA (RASA1)
ENST00000512763.5:c.1109+177_1109+179delinsTCA (RASA1) ENSP00000422008.1:n.1109+177_1109+179delinsTCA
ENST00000515800.6:c.1610+177_1610+179delinsTCA (RASA1) ENSP00000423395.2:n.1610+177_1610+179delinsTCA
NM_002890.2:c.1610+177_1610+179delinsTCA (RASA1) NP_002881.1:n.1610+177_1610+179delinsTCA
NM_022650.2:c.1079+177_1079+179delinsTCA (RASA1) NP_072179.1:n.1079+177_1079+179delinsTCA
XM_011543525.1:c.1610+177_1610+179delinsTCA (RASA1) XP_011541827.1:n.1610+177_1610+179delinsTCA
XM_011543526.1:c.1610+177_1610+179delinsTCA (RASA1) XP_011541828.1:n.1610+177_1610+179delinsTCA
XM_011543527.1:c.1610+177_1610+179delinsTCA (RASA1) XP_011541829.1:n.1610+177_1610+179delinsTCA
NM_001364075.1:c.933+31361_933+31363delinsTGA (CCNH) NP_001351004.1:n.933+31361_933+31363delinsTGA
NR_157068.1:n.1447+29087_1447+29089delinsTGA (CCNH)
NR_157069.1:n.1040+29087_1040+29089delinsTGA (CCNH)
NR_157070.1:n.1204+29087_1204+29089delinsTGA (CCNH)
XM_011543525.2:c.1610+177_1610+179delinsTCA (RASA1) XP_011541827.1:n.1610+177_1610+179delinsTCA
XM_011543527.3:c.1610+177_1610+179delinsTCA (RASA1) XP_011541829.1:n.1610+177_1610+179delinsTCA
NM_001364075.2:c.933+31361_933+31363delinsTGA (CCNH) NP_001351004.1:n.933+31361_933+31363delinsTGA
NM_002890.3:c.1610+177_1610+179delinsTCA (RASA1) MANE Select NP_002881.1:n.1610+177_1610+179delinsTCA
NR_157068.2:n.1447+29087_1447+29089delinsTGA (CCNH)
NR_157069.2:n.1040+29087_1040+29089delinsTGA (CCNH)
NR_157070.2:n.1204+29087_1204+29089delinsTGA (CCNH)
NM_022650.3:c.1079+177_1079+179delinsTCA (RASA1) NP_072179.1:n.1079+177_1079+179delinsTCA