Canonical Allele Identifier: CA2695204784

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389528dup , CM000667.2:g.87389528dup	GRCh38
NC_000005.9:g.86685345dup , CM000667.1:g.86685345dup	GRCh37
NC_000005.8:g.86721101dup	NCBI36
NG_011650.1:g.126195dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.3060+1dup (RASA1)
ENST00000645953.1:c.*90+3243dup (CCNH)	ENSP00000494460.1:n.*90+3243dup
ENST00000646883.1:c.254+3243dup (CCNH)
ENST00000274376.10:c.3060+1dup (RASA1)
ENST00000456692.6:c.2529+1dup (RASA1)
ENST00000506290.1:c.2562+1dup (RASA1)
ENST00000512763.5:c.2559+1dup (RASA1)
ENST00000515800.6:c.*1675+1dup (RASA1)
NM_002890.2:c.3060+1dup (RASA1)
NM_022650.2:c.2529+1dup (RASA1)
XM_011543525.1:c.2973+1dup (RASA1)
NM_001364075.1:c.933+5517dup (CCNH)	NP_001351004.1:n.933+5517dup
NR_157068.1:n.1447+3243dup (CCNH)
NR_157069.1:n.1040+3243dup (CCNH)
NR_157070.1:n.1204+3243dup (CCNH)
XM_011543525.2:c.2973+1dup (RASA1)
NM_001364075.2:c.933+5517dup (CCNH)	NP_001351004.1:n.933+5517dup
NM_002890.3:c.3060+1dup (RASA1)
NR_157068.2:n.1447+3243dup (CCNH)
NR_157069.2:n.1040+3243dup (CCNH)
NR_157070.2:n.1204+3243dup (CCNH)
NM_022650.3:c.2529+1dup (RASA1)