Canonical Allele Identifier: CA360388691

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86685343A>T (hg19) ; chr5:g.87389526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389526A>T , CM000667.2:g.87389526A>T	GRCh38
NC_000005.9:g.86685343A>T , CM000667.1:g.86685343A>T	GRCh37
NC_000005.8:g.86721099A>T	NCBI36
NG_011650.1:g.126193A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.3059A>T (RASA1) MANE Select	ENSP00000274376.6:p.Gln1020Leu
ENST00000645953.1:c.*90+3244T>A (CCNH)	ENSP00000494460.1:n.*90+3244T>A
ENST00000646883.1:c.254+3244T>A (CCNH)
ENST00000274376.10:c.3059A>T (RASA1)	ENSP00000274376.6:p.Gln1020Leu
ENST00000456692.6:c.2528A>T (RASA1)	ENSP00000411221.2:p.Gln843Leu
ENST00000506290.1:c.2561A>T (RASA1)	ENSP00000420905.1:p.Gln854Leu
ENST00000512763.5:c.2558A>T (RASA1)	ENSP00000422008.1:p.Gln853Leu
ENST00000515800.6:c.*1674A>T (RASA1)	ENSP00000423395.2:n.*1674A>T
NM_002890.2:c.3059A>T (RASA1)	NP_002881.1:p.Gln1020Leu
NM_022650.2:c.2528A>T (RASA1)	NP_072179.1:p.Gln843Leu
XM_011543525.1:c.2972A>T (RASA1)	XP_011541827.1:p.Gln991Leu
NM_001364075.1:c.933+5518T>A (CCNH)	NP_001351004.1:n.933+5518T>A
NR_157068.1:n.1447+3244T>A (CCNH)
NR_157069.1:n.1040+3244T>A (CCNH)
NR_157070.1:n.1204+3244T>A (CCNH)
XM_011543525.2:c.2972A>T (RASA1)	XP_011541827.1:p.Gln991Leu
NM_001364075.2:c.933+5518T>A (CCNH)	NP_001351004.1:n.933+5518T>A
NM_002890.3:c.3059A>T (RASA1) MANE Select	NP_002881.1:p.Gln1020Leu
NR_157068.2:n.1447+3244T>A (CCNH)
NR_157069.2:n.1040+3244T>A (CCNH)
NR_157070.2:n.1204+3244T>A (CCNH)
NM_022650.3:c.2528A>T (RASA1)	NP_072179.1:p.Gln843Leu