Canonical Allele Identifier: CA1561579951

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87333291C= , CM000667.2:g.87333291C=	GRCh38
NC_000005.9:g.86629108C= , CM000667.1:g.86629108C=	GRCh37
NC_000005.8:g.86664864C=	NCBI36
NG_011650.1:g.69958C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.853C= (RASA1) MANE Select	ENSP00000274376.6:p.Arg285=
ENST00000645953.1:c.*91-14394G= (CCNH)	ENSP00000494460.1:n.*91-14394G=
ENST00000274376.10:c.853C= (RASA1)	ENSP00000274376.6:p.Arg285=
ENST00000456692.6:c.322C= (RASA1)	ENSP00000411221.2:p.Arg108=
ENST00000506290.1:c.355C= (RASA1)	ENSP00000420905.1:p.Arg119=
ENST00000512763.5:c.352C= (RASA1)	ENSP00000422008.1:p.Arg118=
ENST00000515800.6:c.853C= (RASA1)	ENSP00000423395.2:p.Arg285=
NM_002890.2:c.853C= (RASA1)	NP_002881.1:p.Arg285=
NM_022650.2:c.322C= (RASA1)	NP_072179.1:p.Arg108=
XM_011543525.1:c.853C= (RASA1)	XP_011541827.1:p.Arg285=
XM_011543526.1:c.853C= (RASA1)	XP_011541828.1:p.Arg285=
XM_011543527.1:c.853C= (RASA1)	XP_011541829.1:p.Arg285=
NM_001364075.1:c.934-20496G= (CCNH)	NP_001351004.1:n.934-20496G=
NR_157068.1:n.1448-20496G= (CCNH)
NR_157069.1:n.1041-20496G= (CCNH)
NR_157070.1:n.1205-20496G= (CCNH)
XM_011543525.2:c.853C= (RASA1)	XP_011541827.1:p.Arg285=
XM_011543527.3:c.853C= (RASA1)	XP_011541829.1:p.Arg285=
NM_001364075.2:c.934-20496G= (CCNH)	NP_001351004.1:n.934-20496G=
NM_002890.3:c.853C= (RASA1) MANE Select	NP_002881.1:p.Arg285=
NR_157068.2:n.1448-20496G= (CCNH)
NR_157069.2:n.1041-20496G= (CCNH)
NR_157070.2:n.1205-20496G= (CCNH)
NM_022650.3:c.322C= (RASA1)	NP_072179.1:p.Arg108=