Canonical Allele Identifier: CA1561597659

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87379706C= , CM000667.2:g.87379706C=	GRCh38
NC_000005.9:g.86675523C= , CM000667.1:g.86675523C=	GRCh37
NC_000005.8:g.86711279C=	NCBI36
NG_011650.1:g.116373C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2488-29C= (RASA1) MANE Select	ENSP00000274376.6:n.2488-29C=
ENST00000645953.1:c.*90+13064G= (CCNH)	ENSP00000494460.1:n.*90+13064G=
ENST00000646883.1:c.255-3188G= (CCNH)
ENST00000274376.10:c.2488-29C= (RASA1)	ENSP00000274376.6:n.2488-29C=
ENST00000456692.6:c.1957-29C= (RASA1)	ENSP00000411221.2:n.1957-29C=
ENST00000506290.1:c.1990-29C= (RASA1)	ENSP00000420905.1:n.1990-29C=
ENST00000512763.5:c.1987-29C= (RASA1)	ENSP00000422008.1:n.1987-29C=
ENST00000515800.6:c.*1013-29C= (RASA1)	ENSP00000423395.2:n.*1013-29C=
NM_002890.2:c.2488-29C= (RASA1)	NP_002881.1:n.2488-29C=
NM_022650.2:c.1957-29C= (RASA1)	NP_072179.1:n.1957-29C=
XM_011543525.1:c.2488-29C= (RASA1)	XP_011541827.1:n.2488-29C=
XM_011543526.1:c.2488-29C= (RASA1)	XP_011541828.1:n.2488-29C=
NM_001364075.1:c.933+15338G= (CCNH)	NP_001351004.1:n.933+15338G=
NR_157068.1:n.1447+13064G= (CCNH)
NR_157069.1:n.1040+13064G= (CCNH)
NR_157070.1:n.1204+13064G= (CCNH)
XM_011543525.2:c.2488-29C= (RASA1)	XP_011541827.1:n.2488-29C=
NM_001364075.2:c.933+15338G= (CCNH)	NP_001351004.1:n.933+15338G=
NM_002890.3:c.2488-29C= (RASA1) MANE Select	NP_002881.1:n.2488-29C=
NR_157068.2:n.1447+13064G= (CCNH)
NR_157069.2:n.1040+13064G= (CCNH)
NR_157070.2:n.1204+13064G= (CCNH)
NM_022650.3:c.1957-29C= (RASA1)	NP_072179.1:n.1957-29C=