Canonical Allele Identifier: CA2580073681

Gene: RASA1 CCNH

Linked Data

• ClinVar Variation Id: 2003753
• ClinVar RCV Id: RCV002811415

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87333337_87333340del , CM000667.2:g.87333337_87333340del	GRCh38
NC_000005.9:g.86629154_86629157del , CM000667.1:g.86629154_86629157del	GRCh37
NC_000005.8:g.86664910_86664913del	NCBI36
NG_011650.1:g.70004_70007del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.899_899+3del (RASA1)
ENST00000645953.1:c.*91-14442_*91-14439del (CCNH)	ENSP00000494460.1:n.*91-14442_*91-14439del
ENST00000274376.10:c.899_899+3del (RASA1)
ENST00000456692.6:c.368_368+3del (RASA1)
ENST00000506290.1:c.401_401+3del (RASA1)
ENST00000512763.5:c.398_398+3del (RASA1)
ENST00000515800.6:c.899_899+3del (RASA1)
NM_002890.2:c.899_899+3del (RASA1)
NM_022650.2:c.368_368+3del (RASA1)
XM_011543525.1:c.899_899+3del (RASA1)
XM_011543526.1:c.899_899+3del (RASA1)
XM_011543527.1:c.899_899+3del (RASA1)
NM_001364075.1:c.934-20544_934-20541del (CCNH)	NP_001351004.1:n.934-20544_934-20541del
NR_157068.1:n.1448-20544_1448-20541del (CCNH)
NR_157069.1:n.1041-20544_1041-20541del (CCNH)
NR_157070.1:n.1205-20544_1205-20541del (CCNH)
XM_011543525.2:c.899_899+3del (RASA1)
XM_011543527.3:c.899_899+3del (RASA1)
NM_001364075.2:c.934-20544_934-20541del (CCNH)	NP_001351004.1:n.934-20544_934-20541del
NM_002890.3:c.899_899+3del (RASA1)
NR_157068.2:n.1448-20544_1448-20541del (CCNH)
NR_157069.2:n.1041-20544_1041-20541del (CCNH)
NR_157070.2:n.1205-20544_1205-20541del (CCNH)
NM_022650.3:c.368_368+3del (RASA1)