Canonical Allele Identifier: CA2578363895

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87331246_87331249del , CM000667.2:g.87331246_87331249del GRCh38
NC_000005.9:g.86627063_86627066del , CM000667.1:g.86627063_86627066del GRCh37
NC_000005.8:g.86662819_86662822del NCBI36
NG_011650.1:g.67913_67916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.540-102_540-99del (RASA1) MANE Select ENSP00000274376.6:n.540-102_540-99del
ENST00000645953.1:c.*91-12351_*91-12348del (CCNH) ENSP00000494460.1:n.*91-12351_*91-12348del
ENST00000274376.10:c.540-102_540-99del (RASA1) ENSP00000274376.6:n.540-102_540-99del
ENST00000456692.6:c.9-102_9-99del (RASA1) ENSP00000411221.2:n.9-102_9-99del
ENST00000506290.1:c.42-102_42-99del (RASA1) ENSP00000420905.1:n.42-102_42-99del
ENST00000512763.5:c.39-102_39-99del (RASA1) ENSP00000422008.1:n.39-102_39-99del
ENST00000515800.6:c.540-102_540-99del (RASA1) ENSP00000423395.2:n.540-102_540-99del
NM_002890.2:c.540-102_540-99del (RASA1) NP_002881.1:n.540-102_540-99del
NM_022650.2:c.9-102_9-99del (RASA1) NP_072179.1:n.9-102_9-99del
XM_011543525.1:c.540-102_540-99del (RASA1) XP_011541827.1:n.540-102_540-99del
XM_011543526.1:c.540-102_540-99del (RASA1) XP_011541828.1:n.540-102_540-99del
XM_011543527.1:c.540-102_540-99del (RASA1) XP_011541829.1:n.540-102_540-99del
NM_001364075.1:c.934-18453_934-18450del (CCNH) NP_001351004.1:n.934-18453_934-18450del
NR_157068.1:n.1448-18453_1448-18450del (CCNH)
NR_157069.1:n.1041-18453_1041-18450del (CCNH)
NR_157070.1:n.1205-18453_1205-18450del (CCNH)
XM_011543525.2:c.540-102_540-99del (RASA1) XP_011541827.1:n.540-102_540-99del
XM_011543527.3:c.540-102_540-99del (RASA1) XP_011541829.1:n.540-102_540-99del
NM_001364075.2:c.934-18453_934-18450del (CCNH) NP_001351004.1:n.934-18453_934-18450del
NM_002890.3:c.540-102_540-99del (RASA1) MANE Select NP_002881.1:n.540-102_540-99del
NR_157068.2:n.1448-18453_1448-18450del (CCNH)
NR_157069.2:n.1041-18453_1041-18450del (CCNH)
NR_157070.2:n.1205-18453_1205-18450del (CCNH)
NM_022650.3:c.9-102_9-99del (RASA1) NP_072179.1:n.9-102_9-99del