Canonical Allele Identifier: CA445184130

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86627312T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.687T>C (RASA1) MANE Select	ENSP00000274376.6:p.His229=
ENST00000645953.1:c.*91-12598A>G (CCNH)	ENSP00000494460.1:n.*91-12598A>G
ENST00000274376.10:c.687T>C (RASA1)	ENSP00000274376.6:p.His229=
ENST00000456692.6:c.156T>C (RASA1)	ENSP00000411221.2:p.His52=
ENST00000506290.1:c.189T>C (RASA1)	ENSP00000420905.1:p.His63=
ENST00000512763.5:c.186T>C (RASA1)	ENSP00000422008.1:p.His62=
ENST00000515800.6:c.687T>C (RASA1)	ENSP00000423395.2:p.His229=
NM_002890.2:c.687T>C (RASA1)	NP_002881.1:p.His229=
NM_022650.2:c.156T>C (RASA1)	NP_072179.1:p.His52=
XM_011543525.1:c.687T>C (RASA1)	XP_011541827.1:p.His229=
XM_011543526.1:c.687T>C (RASA1)	XP_011541828.1:p.His229=
XM_011543527.1:c.687T>C (RASA1)	XP_011541829.1:p.His229=
NM_001364075.1:c.934-18700A>G (CCNH)	NP_001351004.1:n.934-18700A>G
NR_157068.1:n.1448-18700A>G (CCNH)
NR_157069.1:n.1041-18700A>G (CCNH)
NR_157070.1:n.1205-18700A>G (CCNH)
XM_011543525.2:c.687T>C (RASA1)	XP_011541827.1:p.His229=
XM_011543527.3:c.687T>C (RASA1)	XP_011541829.1:p.His229=
NM_001364075.2:c.934-18700A>G (CCNH)	NP_001351004.1:n.934-18700A>G
NM_002890.3:c.687T>C (RASA1) MANE Select	NP_002881.1:p.His229=
NR_157068.2:n.1448-18700A>G (CCNH)
NR_157069.2:n.1041-18700A>G (CCNH)
NR_157070.2:n.1205-18700A>G (CCNH)
NM_022650.3:c.156T>C (RASA1)	NP_072179.1:p.His52=