Canonical Allele Identifier: CA1561579316

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331692_87331695delinsATAT , CM000667.2:g.87331692_87331695delinsATAT GRCh38
NC_000005.9:g.86627509_86627512delinsATAT , CM000667.1:g.86627509_86627512delinsATAT GRCh37
NC_000005.8:g.86663265_86663268delinsATAT NCBI36
NG_011650.1:g.68359_68362delinsATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.692+192_692+195delinsATAT (RASA1) MANE Select ENSP00000274376.6:n.692+192_692+195delinsATAT
ENST00000645953.1:c.*91-12798_*91-12795delinsATAT (CCNH) ENSP00000494460.1:n.*91-12798_*91-12795delinsATAT
ENST00000274376.10:c.692+192_692+195delinsATAT (RASA1) ENSP00000274376.6:n.692+192_692+195delinsATAT
ENST00000456692.6:c.161+192_161+195delinsATAT (RASA1) ENSP00000411221.2:n.161+192_161+195delinsATAT
ENST00000506290.1:c.194+192_194+195delinsATAT (RASA1) ENSP00000420905.1:n.194+192_194+195delinsATAT
ENST00000512763.5:c.191+192_191+195delinsATAT (RASA1) ENSP00000422008.1:n.191+192_191+195delinsATAT
ENST00000515800.6:c.692+192_692+195delinsATAT (RASA1) ENSP00000423395.2:n.692+192_692+195delinsATAT
NM_002890.2:c.692+192_692+195delinsATAT (RASA1) NP_002881.1:n.692+192_692+195delinsATAT
NM_022650.2:c.161+192_161+195delinsATAT (RASA1) NP_072179.1:n.161+192_161+195delinsATAT
XM_011543525.1:c.692+192_692+195delinsATAT (RASA1) XP_011541827.1:n.692+192_692+195delinsATAT
XM_011543526.1:c.692+192_692+195delinsATAT (RASA1) XP_011541828.1:n.692+192_692+195delinsATAT
XM_011543527.1:c.692+192_692+195delinsATAT (RASA1) XP_011541829.1:n.692+192_692+195delinsATAT
NM_001364075.1:c.934-18900_934-18897delinsATAT (CCNH) NP_001351004.1:n.934-18900_934-18897delinsATAT
NR_157068.1:n.1448-18900_1448-18897delinsATAT (CCNH)
NR_157069.1:n.1041-18900_1041-18897delinsATAT (CCNH)
NR_157070.1:n.1205-18900_1205-18897delinsATAT (CCNH)
XM_011543525.2:c.692+192_692+195delinsATAT (RASA1) XP_011541827.1:n.692+192_692+195delinsATAT
XM_011543527.3:c.692+192_692+195delinsATAT (RASA1) XP_011541829.1:n.692+192_692+195delinsATAT
NM_001364075.2:c.934-18900_934-18897delinsATAT (CCNH) NP_001351004.1:n.934-18900_934-18897delinsATAT
NM_002890.3:c.692+192_692+195delinsATAT (RASA1) MANE Select NP_002881.1:n.692+192_692+195delinsATAT
NR_157068.2:n.1448-18900_1448-18897delinsATAT (CCNH)
NR_157069.2:n.1041-18900_1041-18897delinsATAT (CCNH)
NR_157070.2:n.1205-18900_1205-18897delinsATAT (CCNH)
NM_022650.3:c.161+192_161+195delinsATAT (RASA1) NP_072179.1:n.161+192_161+195delinsATAT