Canonical Allele Identifier: CA360383873

Gene: RASA1 CCNH

Linked Data

• COSMIC: COSM322989
• MyVariant Identifiers: chr5:g.86675613A>G (hg19) ; chr5:g.87379796A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87379796A>G , CM000667.2:g.87379796A>G	GRCh38
NC_000005.9:g.86675613A>G , CM000667.1:g.86675613A>G	GRCh37
NC_000005.8:g.86711369A>G	NCBI36
NG_011650.1:g.116463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2549A>G (RASA1) MANE Select	ENSP00000274376.6:p.Asn850Ser
ENST00000645953.1:c.*90+12974T>C (CCNH)	ENSP00000494460.1:n.*90+12974T>C
ENST00000646883.1:c.255-3278T>C (CCNH)
ENST00000274376.10:c.2549A>G (RASA1)	ENSP00000274376.6:p.Asn850Ser
ENST00000456692.6:c.2018A>G (RASA1)	ENSP00000411221.2:p.Asn673Ser
ENST00000506290.1:c.2051A>G (RASA1)	ENSP00000420905.1:p.Asn684Ser
ENST00000512763.5:c.2048A>G (RASA1)	ENSP00000422008.1:p.Asn683Ser
ENST00000515800.6:c.*1074A>G (RASA1)	ENSP00000423395.2:n.*1074A>G
NM_002890.2:c.2549A>G (RASA1)	NP_002881.1:p.Asn850Ser
NM_022650.2:c.2018A>G (RASA1)	NP_072179.1:p.Asn673Ser
XM_011543525.1:c.2549A>G (RASA1)	XP_011541827.1:p.Asn850Ser
XM_011543526.1:c.2549A>G (RASA1)	XP_011541828.1:p.Asn850Ser
NM_001364075.1:c.933+15248T>C (CCNH)	NP_001351004.1:n.933+15248T>C
NR_157068.1:n.1447+12974T>C (CCNH)
NR_157069.1:n.1040+12974T>C (CCNH)
NR_157070.1:n.1204+12974T>C (CCNH)
XM_011543525.2:c.2549A>G (RASA1)	XP_011541827.1:p.Asn850Ser
NM_001364075.2:c.933+15248T>C (CCNH)	NP_001351004.1:n.933+15248T>C
NM_002890.3:c.2549A>G (RASA1) MANE Select	NP_002881.1:p.Asn850Ser
NR_157068.2:n.1447+12974T>C (CCNH)
NR_157069.2:n.1040+12974T>C (CCNH)
NR_157070.2:n.1204+12974T>C (CCNH)
NM_022650.3:c.2018A>G (RASA1)	NP_072179.1:p.Asn673Ser