Canonical Allele Identifier: CA1561583901

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87374956G= , CM000667.2:g.87374956G=	GRCh38
NC_000005.9:g.86670773G= , CM000667.1:g.86670773G=	GRCh37
NC_000005.8:g.86706529G=	NCBI36
NG_011650.1:g.111623G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.2011+40G= (RASA1) MANE Select	ENSP00000274376.6:n.2011+40G=
ENST00000645953.1:c.*90+17814C= (CCNH)	ENSP00000494460.1:n.*90+17814C=
ENST00000274376.10:c.2011+40G= (RASA1)	ENSP00000274376.6:n.2011+40G=
ENST00000456692.6:c.1480+40G= (RASA1)	ENSP00000411221.2:n.1480+40G=
ENST00000506290.1:c.1513+40G= (RASA1)	ENSP00000420905.1:n.1513+40G=
ENST00000512763.5:c.1510+40G= (RASA1)	ENSP00000422008.1:n.1510+40G=
ENST00000515800.6:c.*536+40G= (RASA1)	ENSP00000423395.2:n.*536+40G=
NM_002890.2:c.2011+40G= (RASA1)	NP_002881.1:n.2011+40G=
NM_022650.2:c.1480+40G= (RASA1)	NP_072179.1:n.1480+40G=
XM_011543525.1:c.2011+40G= (RASA1)	XP_011541827.1:n.2011+40G=
XM_011543526.1:c.2011+40G= (RASA1)	XP_011541828.1:n.2011+40G=
XR_948544.1:n.742+689C=
NM_001364075.1:c.933+20088C= (CCNH)	NP_001351004.1:n.933+20088C=
NR_157068.1:n.1447+17814C= (CCNH)
NR_157069.1:n.1040+17814C= (CCNH)
NR_157070.1:n.1204+17814C= (CCNH)
XM_011543525.2:c.2011+40G= (RASA1)	XP_011541827.1:n.2011+40G=
NM_001364075.2:c.933+20088C= (CCNH)	NP_001351004.1:n.933+20088C=
NM_002890.3:c.2011+40G= (RASA1) MANE Select	NP_002881.1:n.2011+40G=
NR_157068.2:n.1447+17814C= (CCNH)
NR_157069.2:n.1040+17814C= (CCNH)
NR_157070.2:n.1204+17814C= (CCNH)
NM_022650.3:c.1480+40G= (RASA1)	NP_072179.1:n.1480+40G=