Canonical Allele Identifier: CA2559362299

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331609_87331610insCTTACCTAAA , CM000667.2:g.87331609_87331610insCTTACCTAAA GRCh38
NC_000005.9:g.86627426_86627427insCTTACCTAAA , CM000667.1:g.86627426_86627427insCTTACCTAAA GRCh37
NC_000005.8:g.86663182_86663183insCTTACCTAAA NCBI36
NG_011650.1:g.68276_68277insCTTACCTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.692+109_692+110insCTTACCTAAA (RASA1) MANE Select ENSP00000274376.6:n.692+109_692+110insCTTACCTAAA
ENST00000645953.1:c.*91-12712_*91-12711insTTAGGTAAGT (CCNH) ENSP00000494460.1:n.*91-12712_*91-12711insTTAGGTAAGT
ENST00000274376.10:c.692+109_692+110insCTTACCTAAA (RASA1) ENSP00000274376.6:n.692+109_692+110insCTTACCTAAA
ENST00000456692.6:c.161+109_161+110insCTTACCTAAA (RASA1) ENSP00000411221.2:n.161+109_161+110insCTTACCTAAA
ENST00000506290.1:c.194+109_194+110insCTTACCTAAA (RASA1) ENSP00000420905.1:n.194+109_194+110insCTTACCTAAA
ENST00000512763.5:c.191+109_191+110insCTTACCTAAA (RASA1) ENSP00000422008.1:n.191+109_191+110insCTTACCTAAA
ENST00000515800.6:c.692+109_692+110insCTTACCTAAA (RASA1) ENSP00000423395.2:n.692+109_692+110insCTTACCTAAA
NM_002890.2:c.692+109_692+110insCTTACCTAAA (RASA1) NP_002881.1:n.692+109_692+110insCTTACCTAAA
NM_022650.2:c.161+109_161+110insCTTACCTAAA (RASA1) NP_072179.1:n.161+109_161+110insCTTACCTAAA
XM_011543525.1:c.692+109_692+110insCTTACCTAAA (RASA1) XP_011541827.1:n.692+109_692+110insCTTACCTAAA
XM_011543526.1:c.692+109_692+110insCTTACCTAAA (RASA1) XP_011541828.1:n.692+109_692+110insCTTACCTAAA
XM_011543527.1:c.692+109_692+110insCTTACCTAAA (RASA1) XP_011541829.1:n.692+109_692+110insCTTACCTAAA
NM_001364075.1:c.934-18814_934-18813insTTAGGTAAGT (CCNH) NP_001351004.1:n.934-18814_934-18813insTTAGGTAAGT
NR_157068.1:n.1448-18814_1448-18813insTTAGGTAAGT (CCNH)
NR_157069.1:n.1041-18814_1041-18813insTTAGGTAAGT (CCNH)
NR_157070.1:n.1205-18814_1205-18813insTTAGGTAAGT (CCNH)
XM_011543525.2:c.692+109_692+110insCTTACCTAAA (RASA1) XP_011541827.1:n.692+109_692+110insCTTACCTAAA
XM_011543527.3:c.692+109_692+110insCTTACCTAAA (RASA1) XP_011541829.1:n.692+109_692+110insCTTACCTAAA
NM_001364075.2:c.934-18814_934-18813insTTAGGTAAGT (CCNH) NP_001351004.1:n.934-18814_934-18813insTTAGGTAAGT
NM_002890.3:c.692+109_692+110insCTTACCTAAA (RASA1) MANE Select NP_002881.1:n.692+109_692+110insCTTACCTAAA
NR_157068.2:n.1448-18814_1448-18813insTTAGGTAAGT (CCNH)
NR_157069.2:n.1041-18814_1041-18813insTTAGGTAAGT (CCNH)
NR_157070.2:n.1205-18814_1205-18813insTTAGGTAAGT (CCNH)
NM_022650.3:c.161+109_161+110insCTTACCTAAA (RASA1) NP_072179.1:n.161+109_161+110insCTTACCTAAA