Canonical Allele Identifier: CA360376618

Gene: RASA1 CCNH

Linked Data

• MyVariant Identifiers: chr5:g.86627319T>C (hg19) ; chr5:g.87331502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331502T>C , CM000667.2:g.87331502T>C	GRCh38
NC_000005.9:g.86627319T>C , CM000667.1:g.86627319T>C	GRCh37
NC_000005.8:g.86663075T>C	NCBI36
NG_011650.1:g.68169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.692+2T>C (RASA1) MANE Select	ENSP00000274376.6:n.692+2T>C
ENST00000645953.1:c.*91-12605A>G (CCNH)	ENSP00000494460.1:n.*91-12605A>G
ENST00000274376.10:c.692+2T>C (RASA1)	ENSP00000274376.6:n.692+2T>C
ENST00000456692.6:c.161+2T>C (RASA1)	ENSP00000411221.2:n.161+2T>C
ENST00000506290.1:c.194+2T>C (RASA1)	ENSP00000420905.1:n.194+2T>C
ENST00000512763.5:c.191+2T>C (RASA1)	ENSP00000422008.1:n.191+2T>C
ENST00000515800.6:c.692+2T>C (RASA1)	ENSP00000423395.2:n.692+2T>C
NM_002890.2:c.692+2T>C (RASA1)	NP_002881.1:n.692+2T>C
NM_022650.2:c.161+2T>C (RASA1)	NP_072179.1:n.161+2T>C
XM_011543525.1:c.692+2T>C (RASA1)	XP_011541827.1:n.692+2T>C
XM_011543526.1:c.692+2T>C (RASA1)	XP_011541828.1:n.692+2T>C
XM_011543527.1:c.692+2T>C (RASA1)	XP_011541829.1:n.692+2T>C
NM_001364075.1:c.934-18707A>G (CCNH)	NP_001351004.1:n.934-18707A>G
NR_157068.1:n.1448-18707A>G (CCNH)
NR_157069.1:n.1041-18707A>G (CCNH)
NR_157070.1:n.1205-18707A>G (CCNH)
XM_011543525.2:c.692+2T>C (RASA1)	XP_011541827.1:n.692+2T>C
XM_011543527.3:c.692+2T>C (RASA1)	XP_011541829.1:n.692+2T>C
NM_001364075.2:c.934-18707A>G (CCNH)	NP_001351004.1:n.934-18707A>G
NM_002890.3:c.692+2T>C (RASA1) MANE Select	NP_002881.1:n.692+2T>C
NR_157068.2:n.1448-18707A>G (CCNH)
NR_157069.2:n.1041-18707A>G (CCNH)
NR_157070.2:n.1205-18707A>G (CCNH)
NM_022650.3:c.161+2T>C (RASA1)	NP_072179.1:n.161+2T>C