Canonical Allele Identifier: CA445200227

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86675567T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87379750T>C , CM000667.2:g.87379750T>C	GRCh38
NC_000005.9:g.86675567T>C , CM000667.1:g.86675567T>C	GRCh37
NC_000005.8:g.86711323T>C	NCBI36
NG_011650.1:g.116417T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.2503T>C (RASA1) MANE Select	ENSP00000274376.6:p.Leu835=
ENST00000645953.1:c.*90+13020A>G (CCNH)	ENSP00000494460.1:n.*90+13020A>G
ENST00000646883.1:c.255-3232A>G (CCNH)
ENST00000274376.10:c.2503T>C (RASA1)	ENSP00000274376.6:p.Leu835=
ENST00000456692.6:c.1972T>C (RASA1)	ENSP00000411221.2:p.Leu658=
ENST00000506290.1:c.2005T>C (RASA1)	ENSP00000420905.1:p.Leu669=
ENST00000512763.5:c.2002T>C (RASA1)	ENSP00000422008.1:p.Leu668=
ENST00000515800.6:c.*1028T>C (RASA1)	ENSP00000423395.2:n.*1028T>C
NM_002890.2:c.2503T>C (RASA1)	NP_002881.1:p.Leu835=
NM_022650.2:c.1972T>C (RASA1)	NP_072179.1:p.Leu658=
XM_011543525.1:c.2503T>C (RASA1)	XP_011541827.1:p.Leu835=
XM_011543526.1:c.2503T>C (RASA1)	XP_011541828.1:p.Leu835=
NM_001364075.1:c.933+15294A>G (CCNH)	NP_001351004.1:n.933+15294A>G
NR_157068.1:n.1447+13020A>G (CCNH)
NR_157069.1:n.1040+13020A>G (CCNH)
NR_157070.1:n.1204+13020A>G (CCNH)
XM_011543525.2:c.2503T>C (RASA1)	XP_011541827.1:p.Leu835=
NM_001364075.2:c.933+15294A>G (CCNH)	NP_001351004.1:n.933+15294A>G
NM_002890.3:c.2503T>C (RASA1) MANE Select	NP_002881.1:p.Leu835=
NR_157068.2:n.1447+13020A>G (CCNH)
NR_157069.2:n.1040+13020A>G (CCNH)
NR_157070.2:n.1204+13020A>G (CCNH)
NM_022650.3:c.1972T>C (RASA1)	NP_072179.1:p.Leu658=