Canonical Allele Identifier: CA360376561

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86627312T>A (hg19) ; chr5:g.87331495T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331495T>A , CM000667.2:g.87331495T>A	GRCh38
NC_000005.9:g.86627312T>A , CM000667.1:g.86627312T>A	GRCh37
NC_000005.8:g.86663068T>A	NCBI36
NG_011650.1:g.68162T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.687T>A (RASA1) MANE Select	ENSP00000274376.6:p.His229Gln
ENST00000645953.1:c.*91-12598A>T (CCNH)	ENSP00000494460.1:n.*91-12598A>T
ENST00000274376.10:c.687T>A (RASA1)	ENSP00000274376.6:p.His229Gln
ENST00000456692.6:c.156T>A (RASA1)	ENSP00000411221.2:p.His52Gln
ENST00000506290.1:c.189T>A (RASA1)	ENSP00000420905.1:p.His63Gln
ENST00000512763.5:c.186T>A (RASA1)	ENSP00000422008.1:p.His62Gln
ENST00000515800.6:c.687T>A (RASA1)	ENSP00000423395.2:p.His229Gln
NM_002890.2:c.687T>A (RASA1)	NP_002881.1:p.His229Gln
NM_022650.2:c.156T>A (RASA1)	NP_072179.1:p.His52Gln
XM_011543525.1:c.687T>A (RASA1)	XP_011541827.1:p.His229Gln
XM_011543526.1:c.687T>A (RASA1)	XP_011541828.1:p.His229Gln
XM_011543527.1:c.687T>A (RASA1)	XP_011541829.1:p.His229Gln
NM_001364075.1:c.934-18700A>T (CCNH)	NP_001351004.1:n.934-18700A>T
NR_157068.1:n.1448-18700A>T (CCNH)
NR_157069.1:n.1041-18700A>T (CCNH)
NR_157070.1:n.1205-18700A>T (CCNH)
XM_011543525.2:c.687T>A (RASA1)	XP_011541827.1:p.His229Gln
XM_011543527.3:c.687T>A (RASA1)	XP_011541829.1:p.His229Gln
NM_001364075.2:c.934-18700A>T (CCNH)	NP_001351004.1:n.934-18700A>T
NM_002890.3:c.687T>A (RASA1) MANE Select	NP_002881.1:p.His229Gln
NR_157068.2:n.1448-18700A>T (CCNH)
NR_157069.2:n.1041-18700A>T (CCNH)
NR_157070.2:n.1205-18700A>T (CCNH)
NM_022650.3:c.156T>A (RASA1)	NP_072179.1:p.His52Gln