Canonical Allele Identifier: CA445184051

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86627189A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331372A>G , CM000667.2:g.87331372A>G	GRCh38
NC_000005.9:g.86627189A>G , CM000667.1:g.86627189A>G	GRCh37
NC_000005.8:g.86662945A>G	NCBI36
NG_011650.1:g.68039A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.564A>G (RASA1) MANE Select	ENSP00000274376.6:p.Arg188=
ENST00000645953.1:c.*91-12475T>C (CCNH)	ENSP00000494460.1:n.*91-12475T>C
ENST00000274376.10:c.564A>G (RASA1)	ENSP00000274376.6:p.Arg188=
ENST00000456692.6:c.33A>G (RASA1)	ENSP00000411221.2:p.Arg11=
ENST00000506290.1:c.66A>G (RASA1)	ENSP00000420905.1:p.Arg22=
ENST00000512763.5:c.63A>G (RASA1)	ENSP00000422008.1:p.Arg21=
ENST00000515800.6:c.564A>G (RASA1)	ENSP00000423395.2:p.Arg188=
NM_002890.2:c.564A>G (RASA1)	NP_002881.1:p.Arg188=
NM_022650.2:c.33A>G (RASA1)	NP_072179.1:p.Arg11=
XM_011543525.1:c.564A>G (RASA1)	XP_011541827.1:p.Arg188=
XM_011543526.1:c.564A>G (RASA1)	XP_011541828.1:p.Arg188=
XM_011543527.1:c.564A>G (RASA1)	XP_011541829.1:p.Arg188=
NM_001364075.1:c.934-18577T>C (CCNH)	NP_001351004.1:n.934-18577T>C
NR_157068.1:n.1448-18577T>C (CCNH)
NR_157069.1:n.1041-18577T>C (CCNH)
NR_157070.1:n.1205-18577T>C (CCNH)
XM_011543525.2:c.564A>G (RASA1)	XP_011541827.1:p.Arg188=
XM_011543527.3:c.564A>G (RASA1)	XP_011541829.1:p.Arg188=
NM_001364075.2:c.934-18577T>C (CCNH)	NP_001351004.1:n.934-18577T>C
NM_002890.3:c.564A>G (RASA1) MANE Select	NP_002881.1:p.Arg188=
NR_157068.2:n.1448-18577T>C (CCNH)
NR_157069.2:n.1041-18577T>C (CCNH)
NR_157070.2:n.1205-18577T>C (CCNH)
NM_022650.3:c.33A>G (RASA1)	NP_072179.1:p.Arg11=