Canonical Allele Identifier: CA2674518389

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87385407_87385409del , CM000667.2:g.87385407_87385409del GRCh38
NC_000005.9:g.86681224_86681226del , CM000667.1:g.86681224_86681226del GRCh37
NC_000005.8:g.86716980_86716982del NCBI36
NG_011650.1:g.122074_122076del

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2847+18_2847+20del (RASA1) MANE Select ENSP00000274376.6:n.2847+18_2847+20del
ENST00000645953.1:c.*90+7361_*90+7363del (CCNH) ENSP00000494460.1:n.*90+7361_*90+7363del
ENST00000646883.1:c.254+7361_254+7363del (CCNH)
ENST00000274376.10:c.2847+18_2847+20del (RASA1) ENSP00000274376.6:n.2847+18_2847+20del
ENST00000456692.6:c.2316+18_2316+20del (RASA1) ENSP00000411221.2:n.2316+18_2316+20del
ENST00000506290.1:c.2349+18_2349+20del (RASA1) ENSP00000420905.1:n.2349+18_2349+20del
ENST00000512763.5:c.2346+18_2346+20del (RASA1) ENSP00000422008.1:n.2346+18_2346+20del
ENST00000515800.6:c.*1372+18_*1372+20del (RASA1) ENSP00000423395.2:n.*1372+18_*1372+20del
NM_002890.2:c.2847+18_2847+20del (RASA1) NP_002881.1:n.2847+18_2847+20del
NM_022650.2:c.2316+18_2316+20del (RASA1) NP_072179.1:n.2316+18_2316+20del
XM_011543525.1:c.2760+18_2760+20del (RASA1) XP_011541827.1:n.2760+18_2760+20del
XM_011543526.1:c.2847+18_2847+20del (RASA1) XP_011541828.1:n.2847+18_2847+20del
NM_001364075.1:c.933+9635_933+9637del (CCNH) NP_001351004.1:n.933+9635_933+9637del
NR_157068.1:n.1447+7361_1447+7363del (CCNH)
NR_157069.1:n.1040+7361_1040+7363del (CCNH)
NR_157070.1:n.1204+7361_1204+7363del (CCNH)
XM_011543525.2:c.2760+18_2760+20del (RASA1) XP_011541827.1:n.2760+18_2760+20del
NM_001364075.2:c.933+9635_933+9637del (CCNH) NP_001351004.1:n.933+9635_933+9637del
NM_002890.3:c.2847+18_2847+20del (RASA1) MANE Select NP_002881.1:n.2847+18_2847+20del
NR_157068.2:n.1447+7361_1447+7363del (CCNH)
NR_157069.2:n.1040+7361_1040+7363del (CCNH)
NR_157070.2:n.1204+7361_1204+7363del (CCNH)
NM_022650.3:c.2316+18_2316+20del (RASA1) NP_072179.1:n.2316+18_2316+20del