Canonical Allele Identifier: CA1561583891

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87374926T= , CM000667.2:g.87374926T= GRCh38
NC_000005.9:g.86670743T= , CM000667.1:g.86670743T= GRCh37
NC_000005.8:g.86706499T= NCBI36
NG_011650.1:g.111593T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.2011+10T= (RASA1) MANE Select ENSP00000274376.6:n.2011+10T=
ENST00000645953.1:c.*90+17844A= (CCNH) ENSP00000494460.1:n.*90+17844A=
ENST00000274376.10:c.2011+10T= (RASA1) ENSP00000274376.6:n.2011+10T=
ENST00000456692.6:c.1480+10T= (RASA1) ENSP00000411221.2:n.1480+10T=
ENST00000506290.1:c.1513+10T= (RASA1) ENSP00000420905.1:n.1513+10T=
ENST00000512763.5:c.1510+10T= (RASA1) ENSP00000422008.1:n.1510+10T=
ENST00000515800.6:c.*536+10T= (RASA1) ENSP00000423395.2:n.*536+10T=
NM_002890.2:c.2011+10T= (RASA1) NP_002881.1:n.2011+10T=
NM_022650.2:c.1480+10T= (RASA1) NP_072179.1:n.1480+10T=
XM_011543525.1:c.2011+10T= (RASA1) XP_011541827.1:n.2011+10T=
XM_011543526.1:c.2011+10T= (RASA1) XP_011541828.1:n.2011+10T=
XR_948544.1:n.742+719A=
NM_001364075.1:c.933+20118A= (CCNH) NP_001351004.1:n.933+20118A=
NR_157068.1:n.1447+17844A= (CCNH)
NR_157069.1:n.1040+17844A= (CCNH)
NR_157070.1:n.1204+17844A= (CCNH)
XM_011543525.2:c.2011+10T= (RASA1) XP_011541827.1:n.2011+10T=
NM_001364075.2:c.933+20118A= (CCNH) NP_001351004.1:n.933+20118A=
NM_002890.3:c.2011+10T= (RASA1) MANE Select NP_002881.1:n.2011+10T=
NR_157068.2:n.1447+17844A= (CCNH)
NR_157069.2:n.1040+17844A= (CCNH)
NR_157070.2:n.1204+17844A= (CCNH)
NM_022650.3:c.1480+10T= (RASA1) NP_072179.1:n.1480+10T=