Canonical Allele Identifier: CA445184072

Gene: RASA1 CCNH

Linked Data

• ClinVar Variation Id: 1750831
• ClinVar RCV Id: RCV002356135
• MyVariant Identifiers: chr5:g.86627222G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331405G>A , CM000667.2:g.87331405G>A	GRCh38
NC_000005.9:g.86627222G>A , CM000667.1:g.86627222G>A	GRCh37
NC_000005.8:g.86662978G>A	NCBI36
NG_011650.1:g.68072G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.597G>A (RASA1) MANE Select	ENSP00000274376.6:p.Gly199=
ENST00000645953.1:c.*91-12508C>T (CCNH)	ENSP00000494460.1:n.*91-12508C>T
ENST00000274376.10:c.597G>A (RASA1)	ENSP00000274376.6:p.Gly199=
ENST00000456692.6:c.66G>A (RASA1)	ENSP00000411221.2:p.Gly22=
ENST00000506290.1:c.99G>A (RASA1)	ENSP00000420905.1:p.Gly33=
ENST00000512763.5:c.96G>A (RASA1)	ENSP00000422008.1:p.Gly32=
ENST00000515800.6:c.597G>A (RASA1)	ENSP00000423395.2:p.Gly199=
NM_002890.2:c.597G>A (RASA1)	NP_002881.1:p.Gly199=
NM_022650.2:c.66G>A (RASA1)	NP_072179.1:p.Gly22=
XM_011543525.1:c.597G>A (RASA1)	XP_011541827.1:p.Gly199=
XM_011543526.1:c.597G>A (RASA1)	XP_011541828.1:p.Gly199=
XM_011543527.1:c.597G>A (RASA1)	XP_011541829.1:p.Gly199=
NM_001364075.1:c.934-18610C>T (CCNH)	NP_001351004.1:n.934-18610C>T
NR_157068.1:n.1448-18610C>T (CCNH)
NR_157069.1:n.1041-18610C>T (CCNH)
NR_157070.1:n.1205-18610C>T (CCNH)
XM_011543525.2:c.597G>A (RASA1)	XP_011541827.1:p.Gly199=
XM_011543527.3:c.597G>A (RASA1)	XP_011541829.1:p.Gly199=
NM_001364075.2:c.934-18610C>T (CCNH)	NP_001351004.1:n.934-18610C>T
NM_002890.3:c.597G>A (RASA1) MANE Select	NP_002881.1:p.Gly199=
NR_157068.2:n.1448-18610C>T (CCNH)
NR_157069.2:n.1041-18610C>T (CCNH)
NR_157070.2:n.1205-18610C>T (CCNH)
NM_022650.3:c.66G>A (RASA1)	NP_072179.1:p.Gly22=