Canonical Allele Identifier: CA2674518395

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87385419_87385423del , CM000667.2:g.87385419_87385423del GRCh38
NC_000005.9:g.86681236_86681240del , CM000667.1:g.86681236_86681240del GRCh37
NC_000005.8:g.86716992_86716996del NCBI36
NG_011650.1:g.122086_122090del

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2847+30_2847+34del (RASA1) MANE Select ENSP00000274376.6:n.2847+30_2847+34del
ENST00000645953.1:c.*90+7349_*90+7353del (CCNH) ENSP00000494460.1:n.*90+7349_*90+7353del
ENST00000646883.1:c.254+7349_254+7353del (CCNH)
ENST00000274376.10:c.2847+30_2847+34del (RASA1) ENSP00000274376.6:n.2847+30_2847+34del
ENST00000456692.6:c.2316+30_2316+34del (RASA1) ENSP00000411221.2:n.2316+30_2316+34del
ENST00000506290.1:c.2349+30_2349+34del (RASA1) ENSP00000420905.1:n.2349+30_2349+34del
ENST00000512763.5:c.2346+30_2346+34del (RASA1) ENSP00000422008.1:n.2346+30_2346+34del
ENST00000515800.6:c.*1372+30_*1372+34del (RASA1) ENSP00000423395.2:n.*1372+30_*1372+34del
NM_002890.2:c.2847+30_2847+34del (RASA1) NP_002881.1:n.2847+30_2847+34del
NM_022650.2:c.2316+30_2316+34del (RASA1) NP_072179.1:n.2316+30_2316+34del
XM_011543525.1:c.2760+30_2760+34del (RASA1) XP_011541827.1:n.2760+30_2760+34del
XM_011543526.1:c.2847+30_2847+34del (RASA1) XP_011541828.1:n.2847+30_2847+34del
NM_001364075.1:c.933+9623_933+9627del (CCNH) NP_001351004.1:n.933+9623_933+9627del
NR_157068.1:n.1447+7349_1447+7353del (CCNH)
NR_157069.1:n.1040+7349_1040+7353del (CCNH)
NR_157070.1:n.1204+7349_1204+7353del (CCNH)
XM_011543525.2:c.2760+30_2760+34del (RASA1) XP_011541827.1:n.2760+30_2760+34del
NM_001364075.2:c.933+9623_933+9627del (CCNH) NP_001351004.1:n.933+9623_933+9627del
NM_002890.3:c.2847+30_2847+34del (RASA1) MANE Select NP_002881.1:n.2847+30_2847+34del
NR_157068.2:n.1447+7349_1447+7353del (CCNH)
NR_157069.2:n.1040+7349_1040+7353del (CCNH)
NR_157070.2:n.1204+7349_1204+7353del (CCNH)
NM_022650.3:c.2316+30_2316+34del (RASA1) NP_072179.1:n.2316+30_2316+34del