Canonical Allele Identifier: CA1561579188

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331399G= , CM000667.2:g.87331399G=	GRCh38
NC_000005.9:g.86627216G= , CM000667.1:g.86627216G=	GRCh37
NC_000005.8:g.86662972G=	NCBI36
NG_011650.1:g.68066G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.591G= (RASA1) MANE Select	ENSP00000274376.6:p.Gln197=
ENST00000645953.1:c.*91-12502C= (CCNH)	ENSP00000494460.1:n.*91-12502C=
ENST00000274376.10:c.591G= (RASA1)	ENSP00000274376.6:p.Gln197=
ENST00000456692.6:c.60G= (RASA1)	ENSP00000411221.2:p.Gln20=
ENST00000506290.1:c.93G= (RASA1)	ENSP00000420905.1:p.Gln31=
ENST00000512763.5:c.90G= (RASA1)	ENSP00000422008.1:p.Gln30=
ENST00000515800.6:c.591G= (RASA1)	ENSP00000423395.2:p.Gln197=
NM_002890.2:c.591G= (RASA1)	NP_002881.1:p.Gln197=
NM_022650.2:c.60G= (RASA1)	NP_072179.1:p.Gln20=
XM_011543525.1:c.591G= (RASA1)	XP_011541827.1:p.Gln197=
XM_011543526.1:c.591G= (RASA1)	XP_011541828.1:p.Gln197=
XM_011543527.1:c.591G= (RASA1)	XP_011541829.1:p.Gln197=
NM_001364075.1:c.934-18604C= (CCNH)	NP_001351004.1:n.934-18604C=
NR_157068.1:n.1448-18604C= (CCNH)
NR_157069.1:n.1041-18604C= (CCNH)
NR_157070.1:n.1205-18604C= (CCNH)
XM_011543525.2:c.591G= (RASA1)	XP_011541827.1:p.Gln197=
XM_011543527.3:c.591G= (RASA1)	XP_011541829.1:p.Gln197=
NM_001364075.2:c.934-18604C= (CCNH)	NP_001351004.1:n.934-18604C=
NM_002890.3:c.591G= (RASA1) MANE Select	NP_002881.1:p.Gln197=
NR_157068.2:n.1448-18604C= (CCNH)
NR_157069.2:n.1041-18604C= (CCNH)
NR_157070.2:n.1205-18604C= (CCNH)
NM_022650.3:c.60G= (RASA1)	NP_072179.1:p.Gln20=