Canonical Allele Identifier: CA1561597825

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87379775C= , CM000667.2:g.87379775C=	GRCh38
NC_000005.9:g.86675592C= , CM000667.1:g.86675592C=	GRCh37
NC_000005.8:g.86711348C=	NCBI36
NG_011650.1:g.116442C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2528C= (RASA1) MANE Select	ENSP00000274376.6:p.Thr843=
ENST00000645953.1:c.*90+12995G= (CCNH)	ENSP00000494460.1:n.*90+12995G=
ENST00000646883.1:c.255-3257G= (CCNH)
ENST00000274376.10:c.2528C= (RASA1)	ENSP00000274376.6:p.Thr843=
ENST00000456692.6:c.1997C= (RASA1)	ENSP00000411221.2:p.Thr666=
ENST00000506290.1:c.2030C= (RASA1)	ENSP00000420905.1:p.Thr677=
ENST00000512763.5:c.2027C= (RASA1)	ENSP00000422008.1:p.Thr676=
ENST00000515800.6:c.*1053C= (RASA1)	ENSP00000423395.2:n.*1053C=
NM_002890.2:c.2528C= (RASA1)	NP_002881.1:p.Thr843=
NM_022650.2:c.1997C= (RASA1)	NP_072179.1:p.Thr666=
XM_011543525.1:c.2528C= (RASA1)	XP_011541827.1:p.Thr843=
XM_011543526.1:c.2528C= (RASA1)	XP_011541828.1:p.Thr843=
NM_001364075.1:c.933+15269G= (CCNH)	NP_001351004.1:n.933+15269G=
NR_157068.1:n.1447+12995G= (CCNH)
NR_157069.1:n.1040+12995G= (CCNH)
NR_157070.1:n.1204+12995G= (CCNH)
XM_011543525.2:c.2528C= (RASA1)	XP_011541827.1:p.Thr843=
NM_001364075.2:c.933+15269G= (CCNH)	NP_001351004.1:n.933+15269G=
NM_002890.3:c.2528C= (RASA1) MANE Select	NP_002881.1:p.Thr843=
NR_157068.2:n.1447+12995G= (CCNH)
NR_157069.2:n.1040+12995G= (CCNH)
NR_157070.2:n.1204+12995G= (CCNH)
NM_022650.3:c.1997C= (RASA1)	NP_072179.1:p.Thr666=