Canonical Allele Identifier: CA2674518377

Gene: RASA1 CCNH

Linked Data

• gnomAD v4: 5-87385290-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87385292_87385293del , CM000667.2:g.87385292_87385293del	GRCh38
NC_000005.9:g.86681109_86681110del , CM000667.1:g.86681109_86681110del	GRCh37
NC_000005.8:g.86716865_86716866del	NCBI36
NG_011650.1:g.121959_121960del

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.2759-9_2759-8del (RASA1) MANE Select	ENSP00000274376.6:n.2759-9_2759-8del
ENST00000645953.1:c.*90+7478_*90+7479del (CCNH)	ENSP00000494460.1:n.*90+7478_*90+7479del
ENST00000646883.1:c.254+7478_254+7479del (CCNH)
ENST00000274376.10:c.2759-9_2759-8del (RASA1)	ENSP00000274376.6:n.2759-9_2759-8del
ENST00000456692.6:c.2228-9_2228-8del (RASA1)	ENSP00000411221.2:n.2228-9_2228-8del
ENST00000506290.1:c.2261-9_2261-8del (RASA1)	ENSP00000420905.1:n.2261-9_2261-8del
ENST00000512763.5:c.2258-9_2258-8del (RASA1)	ENSP00000422008.1:n.2258-9_2258-8del
ENST00000515800.6:c.*1284-9_*1284-8del (RASA1)	ENSP00000423395.2:n.*1284-9_*1284-8del
NM_002890.2:c.2759-9_2759-8del (RASA1)	NP_002881.1:n.2759-9_2759-8del
NM_022650.2:c.2228-9_2228-8del (RASA1)	NP_072179.1:n.2228-9_2228-8del
XM_011543525.1:c.2672-9_2672-8del (RASA1)	XP_011541827.1:n.2672-9_2672-8del
XM_011543526.1:c.2759-9_2759-8del (RASA1)	XP_011541828.1:n.2759-9_2759-8del
NM_001364075.1:c.933+9752_933+9753del (CCNH)	NP_001351004.1:n.933+9752_933+9753del
NR_157068.1:n.1447+7478_1447+7479del (CCNH)
NR_157069.1:n.1040+7478_1040+7479del (CCNH)
NR_157070.1:n.1204+7478_1204+7479del (CCNH)
XM_011543525.2:c.2672-9_2672-8del (RASA1)	XP_011541827.1:n.2672-9_2672-8del
NM_001364075.2:c.933+9752_933+9753del (CCNH)	NP_001351004.1:n.933+9752_933+9753del
NM_002890.3:c.2759-9_2759-8del (RASA1) MANE Select	NP_002881.1:n.2759-9_2759-8del
NR_157068.2:n.1447+7478_1447+7479del (CCNH)
NR_157069.2:n.1040+7478_1040+7479del (CCNH)
NR_157070.2:n.1204+7478_1204+7479del (CCNH)
NM_022650.3:c.2228-9_2228-8del (RASA1)	NP_072179.1:n.2228-9_2228-8del