Canonical Allele Identifier: CA1561579207

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331440G= , CM000667.2:g.87331440G=	GRCh38
NC_000005.9:g.86627257G= , CM000667.1:g.86627257G=	GRCh37
NC_000005.8:g.86663013G=	NCBI36
NG_011650.1:g.68107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.632G= (RASA1) MANE Select	ENSP00000274376.6:p.Arg211=
ENST00000645953.1:c.*91-12543C= (CCNH)	ENSP00000494460.1:n.*91-12543C=
ENST00000274376.10:c.632G= (RASA1)	ENSP00000274376.6:p.Arg211=
ENST00000456692.6:c.101G= (RASA1)	ENSP00000411221.2:p.Arg34=
ENST00000506290.1:c.134G= (RASA1)	ENSP00000420905.1:p.Arg45=
ENST00000512763.5:c.131G= (RASA1)	ENSP00000422008.1:p.Arg44=
ENST00000515800.6:c.632G= (RASA1)	ENSP00000423395.2:p.Arg211=
NM_002890.2:c.632G= (RASA1)	NP_002881.1:p.Arg211=
NM_022650.2:c.101G= (RASA1)	NP_072179.1:p.Arg34=
XM_011543525.1:c.632G= (RASA1)	XP_011541827.1:p.Arg211=
XM_011543526.1:c.632G= (RASA1)	XP_011541828.1:p.Arg211=
XM_011543527.1:c.632G= (RASA1)	XP_011541829.1:p.Arg211=
NM_001364075.1:c.934-18645C= (CCNH)	NP_001351004.1:n.934-18645C=
NR_157068.1:n.1448-18645C= (CCNH)
NR_157069.1:n.1041-18645C= (CCNH)
NR_157070.1:n.1205-18645C= (CCNH)
XM_011543525.2:c.632G= (RASA1)	XP_011541827.1:p.Arg211=
XM_011543527.3:c.632G= (RASA1)	XP_011541829.1:p.Arg211=
NM_001364075.2:c.934-18645C= (CCNH)	NP_001351004.1:n.934-18645C=
NM_002890.3:c.632G= (RASA1) MANE Select	NP_002881.1:p.Arg211=
NR_157068.2:n.1448-18645C= (CCNH)
NR_157069.2:n.1041-18645C= (CCNH)
NR_157070.2:n.1205-18645C= (CCNH)
NM_022650.3:c.101G= (RASA1)	NP_072179.1:p.Arg34=