Canonical Allele Identifier: CA1561579171

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331329_87331331delinsTTC , CM000667.2:g.87331329_87331331delinsTTC GRCh38
NC_000005.9:g.86627146_86627148delinsTTC , CM000667.1:g.86627146_86627148delinsTTC GRCh37
NC_000005.8:g.86662902_86662904delinsTTC NCBI36
NG_011650.1:g.67996_67998delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.540-19_540-17delinsTTC (RASA1) MANE Select ENSP00000274376.6:n.540-19_540-17delinsTT...
ENST00000645953.1:c.*91-12434_*91-12432delinsGAA (CCNH) ENSP00000494460.1:n.*91-12434_*91-12432de...
ENST00000274376.10:c.540-19_540-17delinsTTC (RASA1) ENSP00000274376.6:n.540-19_540-17delinsTT...
ENST00000456692.6:c.9-19_9-17delinsTTC (RASA1) ENSP00000411221.2:n.9-19_9-17delinsTTC
ENST00000506290.1:c.42-19_42-17delinsTTC (RASA1) ENSP00000420905.1:n.42-19_42-17delinsTTC
ENST00000512763.5:c.39-19_39-17delinsTTC (RASA1) ENSP00000422008.1:n.39-19_39-17delinsTTC
ENST00000515800.6:c.540-19_540-17delinsTTC (RASA1) ENSP00000423395.2:n.540-19_540-17delinsTT...
NM_002890.2:c.540-19_540-17delinsTTC (RASA1) NP_002881.1:n.540-19_540-17delinsTTC
NM_022650.2:c.9-19_9-17delinsTTC (RASA1) NP_072179.1:n.9-19_9-17delinsTTC
XM_011543525.1:c.540-19_540-17delinsTTC (RASA1) XP_011541827.1:n.540-19_540-17delinsTTC
XM_011543526.1:c.540-19_540-17delinsTTC (RASA1) XP_011541828.1:n.540-19_540-17delinsTTC
XM_011543527.1:c.540-19_540-17delinsTTC (RASA1) XP_011541829.1:n.540-19_540-17delinsTTC
NM_001364075.1:c.934-18536_934-18534delinsGAA (CCNH) NP_001351004.1:n.934-18536_934-18534delin...
NR_157068.1:n.1448-18536_1448-18534delinsGAA (CCNH)
NR_157069.1:n.1041-18536_1041-18534delinsGAA (CCNH)
NR_157070.1:n.1205-18536_1205-18534delinsGAA (CCNH)
XM_011543525.2:c.540-19_540-17delinsTTC (RASA1) XP_011541827.1:n.540-19_540-17delinsTTC
XM_011543527.3:c.540-19_540-17delinsTTC (RASA1) XP_011541829.1:n.540-19_540-17delinsTTC
NM_001364075.2:c.934-18536_934-18534delinsGAA (CCNH) NP_001351004.1:n.934-18536_934-18534delin...
NM_002890.3:c.540-19_540-17delinsTTC (RASA1) MANE Select NP_002881.1:n.540-19_540-17delinsTTC
NR_157068.2:n.1448-18536_1448-18534delinsGAA (CCNH)
NR_157069.2:n.1041-18536_1041-18534delinsGAA (CCNH)
NR_157070.2:n.1205-18536_1205-18534delinsGAA (CCNH)
NM_022650.3:c.9-19_9-17delinsTTC (RASA1) NP_072179.1:n.9-19_9-17delinsTTC