Canonical Allele Identifier: CA1561597794

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87379761_87379764delinsTGAA , CM000667.2:g.87379761_87379764delinsTGAA GRCh38
NC_000005.9:g.86675578_86675581delinsTGAA , CM000667.1:g.86675578_86675581delinsTGAA GRCh37
NC_000005.8:g.86711334_86711337delinsTGAA NCBI36
NG_011650.1:g.116428_116431delinsTGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2514_2517delinsTGAA (RASA1) MANE Select ENSP00000274376.6:p.Asn838=
ENST00000645953.1:c.*90+13006_*90+13009delinsTTCA (CCNH) ENSP00000494460.1:n.*90+13006_*90+13009delinsTTCA
ENST00000646883.1:c.255-3246_255-3243delinsTTCA (CCNH)
ENST00000274376.10:c.2514_2517delinsTGAA (RASA1) ENSP00000274376.6:p.Asn838=
ENST00000456692.6:c.1983_1986delinsTGAA (RASA1) ENSP00000411221.2:p.Asn661=
ENST00000506290.1:c.2016_2019delinsTGAA (RASA1) ENSP00000420905.1:p.Asn672=
ENST00000512763.5:c.2013_2016delinsTGAA (RASA1) ENSP00000422008.1:p.Asn671=
ENST00000515800.6:c.*1039_*1042delinsTGAA (RASA1) ENSP00000423395.2:n.*1039_*1042delinsTGAA
NM_002890.2:c.2514_2517delinsTGAA (RASA1) NP_002881.1:p.Asn838=
NM_022650.2:c.1983_1986delinsTGAA (RASA1) NP_072179.1:p.Asn661=
XM_011543525.1:c.2514_2517delinsTGAA (RASA1) XP_011541827.1:p.Asn838=
XM_011543526.1:c.2514_2517delinsTGAA (RASA1) XP_011541828.1:p.Asn838=
NM_001364075.1:c.933+15280_933+15283delinsTTCA (CCNH) NP_001351004.1:n.933+15280_933+15283delinsTTCA
NR_157068.1:n.1447+13006_1447+13009delinsTTCA (CCNH)
NR_157069.1:n.1040+13006_1040+13009delinsTTCA (CCNH)
NR_157070.1:n.1204+13006_1204+13009delinsTTCA (CCNH)
XM_011543525.2:c.2514_2517delinsTGAA (RASA1) XP_011541827.1:p.Asn838=
NM_001364075.2:c.933+15280_933+15283delinsTTCA (CCNH) NP_001351004.1:n.933+15280_933+15283delinsTTCA
NM_002890.3:c.2514_2517delinsTGAA (RASA1) MANE Select NP_002881.1:p.Asn838=
NR_157068.2:n.1447+13006_1447+13009delinsTTCA (CCNH)
NR_157069.2:n.1040+13006_1040+13009delinsTTCA (CCNH)
NR_157070.2:n.1204+13006_1204+13009delinsTTCA (CCNH)
NM_022650.3:c.1983_1986delinsTGAA (RASA1) NP_072179.1:p.Asn661=