Canonical Allele Identifier: CA2739289435

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87379778dup , CM000667.2:g.87379778dup	GRCh38
NC_000005.9:g.86675595dup , CM000667.1:g.86675595dup	GRCh37
NC_000005.8:g.86711351dup	NCBI36
NG_011650.1:g.116445dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2531dup (RASA1) MANE Select	ENSP00000274376.6:p.Asn844LysfsTer?
ENST00000645953.1:c.*90+12993dup (CCNH)	ENSP00000494460.1:n.*90+12993dup
ENST00000646883.1:c.255-3259dup (CCNH)
ENST00000274376.10:c.2531dup (RASA1)	ENSP00000274376.6:p.Asn844LysfsTer?
ENST00000456692.6:c.2000dup (RASA1)	ENSP00000411221.2:p.Asn667LysfsTer?
ENST00000506290.1:c.2033dup (RASA1)	ENSP00000420905.1:p.Asn678LysfsTer?
ENST00000512763.5:c.2030dup (RASA1)	ENSP00000422008.1:p.Asn677LysfsTer?
ENST00000515800.6:c.*1056dup (RASA1)	ENSP00000423395.2:n.*1056dup
NM_002890.2:c.2531dup (RASA1)	NP_002881.1:p.Asn844LysfsTer?
NM_022650.2:c.2000dup (RASA1)	NP_072179.1:p.Asn667LysfsTer?
XM_011543525.1:c.2531dup (RASA1)	XP_011541827.1:p.Asn844LysfsTer?
XM_011543526.1:c.2531dup (RASA1)	XP_011541828.1:p.Asn844LysfsTer?
NM_001364075.1:c.933+15267dup (CCNH)	NP_001351004.1:n.933+15267dup
NR_157068.1:n.1447+12993dup (CCNH)
NR_157069.1:n.1040+12993dup (CCNH)
NR_157070.1:n.1204+12993dup (CCNH)
XM_011543525.2:c.2531dup (RASA1)	XP_011541827.1:p.Asn844LysfsTer?
NM_001364075.2:c.933+15267dup (CCNH)	NP_001351004.1:n.933+15267dup
NM_002890.3:c.2531dup (RASA1) MANE Select	NP_002881.1:p.Asn844LysfsTer?
NR_157068.2:n.1447+12993dup (CCNH)
NR_157069.2:n.1040+12993dup (CCNH)
NR_157070.2:n.1204+12993dup (CCNH)
NM_022650.3:c.2000dup (RASA1)	NP_072179.1:p.Asn667LysfsTer?