Canonical Allele Identifier: CA2563445024

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87390783A>G , CM000667.2:g.87390783A>G	GRCh38
NC_000005.9:g.86686600A>G , CM000667.1:g.86686600A>G	GRCh37
NC_000005.8:g.86722356A>G	NCBI36
NG_011650.1:g.127450A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002890.3:c.3061-17A>G (RASA1) MANE Select	NP_002881.1:n.3061-17A>G
ENST00000274376.11:c.3061-17A>G (RASA1) MANE Select	ENSP00000274376.6:n.3061-17A>G
NM_001363539.1:c.*2077T>C (CCNH)	NP_001350468.1:n.*2077T>C
NM_001363539.2:c.*2077T>C (CCNH)	NP_001350468.1:n.*2077T>C
NM_001364075.1:c.933+4261T>C (CCNH)	NP_001351004.1:n.933+4261T>C
NM_001364075.2:c.933+4261T>C (CCNH)	NP_001351004.1:n.933+4261T>C
NM_001364076.1:c.*2077T>C (CCNH)	NP_001351005.1:n.*2077T>C
NM_001364076.2:c.*2077T>C (CCNH)	NP_001351005.1:n.*2077T>C
NM_002890.2:c.3061-17A>G (RASA1)	NP_002881.1:n.3061-17A>G
NM_022650.2:c.2530-17A>G (RASA1)	NP_072179.1:n.2530-17A>G
NM_022650.3:c.2530-17A>G (RASA1)	NP_072179.1:n.2530-17A>G
NR_157068.1:n.1447+1987T>C (CCNH)
NR_157068.2:n.1447+1987T>C (CCNH)
NR_157069.1:n.1040+1987T>C (CCNH)
NR_157069.2:n.1040+1987T>C (CCNH)
NR_157070.1:n.1204+1987T>C (CCNH)
NR_157070.2:n.1204+1987T>C (CCNH)
NR_157071.1:n.3027T>C (CCNH)
NR_157071.2:n.3027T>C (CCNH)
ENST00000274376.10:c.3061-17A>G (RASA1)	ENSP00000274376.6:n.3061-17A>G
ENST00000456692.6:c.2530-17A>G (RASA1)	ENSP00000411221.2:n.2530-17A>G
ENST00000506290.1:c.2563-17A>G (RASA1)	ENSP00000420905.1:n.2563-17A>G
ENST00000512763.5:c.2560-17A>G (RASA1)	ENSP00000422008.1:n.2560-17A>G
ENST00000515800.6:c.*1676-17A>G (RASA1)	ENSP00000423395.2:n.*1676-17A>G
ENST00000645953.1:c.*90+1987T>C (CCNH)	ENSP00000494460.1:n.*90+1987T>C
ENST00000646883.1:c.254+1987T>C (CCNH)
XM_011543525.1:c.2974-17A>G (RASA1)	XP_011541827.1:n.2974-17A>G
XM_011543525.2:c.2974-17A>G (RASA1)	XP_011541827.1:n.2974-17A>G