Canonical Allele Identifier: CA2578355171

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87389323_87389325del , CM000667.2:g.87389323_87389325del GRCh38
NC_000005.9:g.86685140_86685142del , CM000667.1:g.86685140_86685142del GRCh37
NC_000005.8:g.86720896_86720898del NCBI36
NG_011650.1:g.125990_125992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.2926-70_2926-68del (RASA1) MANE Select ENSP00000274376.6:n.2926-70_2926-68del
ENST00000645953.1:c.*90+3445_*90+3447del (CCNH) ENSP00000494460.1:n.*90+3445_*90+3447del
ENST00000646883.1:c.254+3445_254+3447del (CCNH)
ENST00000274376.10:c.2926-70_2926-68del (RASA1) ENSP00000274376.6:n.2926-70_2926-68del
ENST00000456692.6:c.2395-70_2395-68del (RASA1) ENSP00000411221.2:n.2395-70_2395-68del
ENST00000506290.1:c.2428-70_2428-68del (RASA1) ENSP00000420905.1:n.2428-70_2428-68del
ENST00000512763.5:c.2425-70_2425-68del (RASA1) ENSP00000422008.1:n.2425-70_2425-68del
ENST00000515800.6:c.*1471_*1473del (RASA1) ENSP00000423395.2:n.*1471_*1473del
NM_002890.2:c.2926-70_2926-68del (RASA1) NP_002881.1:n.2926-70_2926-68del
NM_022650.2:c.2395-70_2395-68del (RASA1) NP_072179.1:n.2395-70_2395-68del
XM_011543525.1:c.2839-70_2839-68del (RASA1) XP_011541827.1:n.2839-70_2839-68del
NM_001364075.1:c.933+5719_933+5721del (CCNH) NP_001351004.1:n.933+5719_933+5721del
NR_157068.1:n.1447+3445_1447+3447del (CCNH)
NR_157069.1:n.1040+3445_1040+3447del (CCNH)
NR_157070.1:n.1204+3445_1204+3447del (CCNH)
XM_011543525.2:c.2839-70_2839-68del (RASA1) XP_011541827.1:n.2839-70_2839-68del
NM_001364075.2:c.933+5719_933+5721del (CCNH) NP_001351004.1:n.933+5719_933+5721del
NM_002890.3:c.2926-70_2926-68del (RASA1) MANE Select NP_002881.1:n.2926-70_2926-68del
NR_157068.2:n.1447+3445_1447+3447del (CCNH)
NR_157069.2:n.1040+3445_1040+3447del (CCNH)
NR_157070.2:n.1204+3445_1204+3447del (CCNH)
NM_022650.3:c.2395-70_2395-68del (RASA1) NP_072179.1:n.2395-70_2395-68del