Canonical Allele Identifier: CA121805349

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87369873T>C , CM000667.2:g.87369873T>C	GRCh38
NC_000005.9:g.86665690T>C , CM000667.1:g.86665690T>C	GRCh37
NC_000005.8:g.86701446T>C	NCBI36
NG_011650.1:g.106540T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002890.3:c.1671T>C (RASA1) MANE Select	NP_002881.1:p.Phe557=
ENST00000274376.11:c.1671T>C (RASA1) MANE Select	ENSP00000274376.6:p.Phe557=
NM_001364075.1:c.933+25171A>G (CCNH)	NP_001351004.1:n.933+25171A>G
NM_001364075.2:c.933+25171A>G (CCNH)	NP_001351004.1:n.933+25171A>G
NM_002890.2:c.1671T>C (RASA1)	NP_002881.1:p.Phe557=
NM_022650.2:c.1140T>C (RASA1)	NP_072179.1:p.Phe380=
NM_022650.3:c.1140T>C (RASA1)	NP_072179.1:p.Phe380=
NR_157068.1:n.1447+22897A>G (CCNH)
NR_157068.2:n.1447+22897A>G (CCNH)
NR_157069.1:n.1040+22897A>G (CCNH)
NR_157069.2:n.1040+22897A>G (CCNH)
NR_157070.1:n.1204+22897A>G (CCNH)
NR_157070.2:n.1204+22897A>G (CCNH)
ENST00000274376.10:c.1671T>C (RASA1)	ENSP00000274376.6:p.Phe557=
ENST00000456692.6:c.1140T>C (RASA1)	ENSP00000411221.2:p.Phe380=
ENST00000506290.1:c.1173T>C (RASA1)	ENSP00000420905.1:p.Phe391=
ENST00000509953.1:n.774T>C (RASA1)
ENST00000512763.5:c.1170T>C (RASA1)	ENSP00000422008.1:p.Phe390=
ENST00000515800.6:c.*196T>C (RASA1)	ENSP00000423395.2:n.*196T>C
ENST00000645953.1:c.*90+22897A>G (CCNH)	ENSP00000494460.1:n.*90+22897A>G
XM_011543525.1:c.1671T>C (RASA1)	XP_011541827.1:p.Phe557=
XM_011543525.2:c.1671T>C (RASA1)	XP_011541827.1:p.Phe557=
XM_011543526.1:c.1671T>C (RASA1)	XP_011541828.1:p.Phe557=