Canonical Allele Identifier: CA1561579320

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331694_87331697delinsATTG , CM000667.2:g.87331694_87331697delinsATTG	GRCh38
NC_000005.9:g.86627511_86627514delinsATTG , CM000667.1:g.86627511_86627514delinsATTG	GRCh37
NC_000005.8:g.86663267_86663270delinsATTG	NCBI36
NG_011650.1:g.68361_68364delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.692+194_692+197delinsATTG (RASA1) MANE Select	ENSP00000274376.6:n.692+194_692+197delinsATTG
ENST00000645953.1:c.*91-12800_*91-12797delinsCAAT (CCNH)	ENSP00000494460.1:n.*91-12800_*91-12797delinsCAAT
ENST00000274376.10:c.692+194_692+197delinsATTG (RASA1)	ENSP00000274376.6:n.692+194_692+197delinsATTG
ENST00000456692.6:c.161+194_161+197delinsATTG (RASA1)	ENSP00000411221.2:n.161+194_161+197delinsATTG
ENST00000506290.1:c.194+194_194+197delinsATTG (RASA1)	ENSP00000420905.1:n.194+194_194+197delinsATTG
ENST00000512763.5:c.191+194_191+197delinsATTG (RASA1)	ENSP00000422008.1:n.191+194_191+197delinsATTG
ENST00000515800.6:c.692+194_692+197delinsATTG (RASA1)	ENSP00000423395.2:n.692+194_692+197delinsATTG
NM_002890.2:c.692+194_692+197delinsATTG (RASA1)	NP_002881.1:n.692+194_692+197delinsATTG
NM_022650.2:c.161+194_161+197delinsATTG (RASA1)	NP_072179.1:n.161+194_161+197delinsATTG
XM_011543525.1:c.692+194_692+197delinsATTG (RASA1)	XP_011541827.1:n.692+194_692+197delinsATTG
XM_011543526.1:c.692+194_692+197delinsATTG (RASA1)	XP_011541828.1:n.692+194_692+197delinsATTG
XM_011543527.1:c.692+194_692+197delinsATTG (RASA1)	XP_011541829.1:n.692+194_692+197delinsATTG
NM_001364075.1:c.934-18902_934-18899delinsCAAT (CCNH)	NP_001351004.1:n.934-18902_934-18899delinsCAAT
NR_157068.1:n.1448-18902_1448-18899delinsCAAT (CCNH)
NR_157069.1:n.1041-18902_1041-18899delinsCAAT (CCNH)
NR_157070.1:n.1205-18902_1205-18899delinsCAAT (CCNH)
XM_011543525.2:c.692+194_692+197delinsATTG (RASA1)	XP_011541827.1:n.692+194_692+197delinsATTG
XM_011543527.3:c.692+194_692+197delinsATTG (RASA1)	XP_011541829.1:n.692+194_692+197delinsATTG
NM_001364075.2:c.934-18902_934-18899delinsCAAT (CCNH)	NP_001351004.1:n.934-18902_934-18899delinsCAAT
NM_002890.3:c.692+194_692+197delinsATTG (RASA1) MANE Select	NP_002881.1:n.692+194_692+197delinsATTG
NR_157068.2:n.1448-18902_1448-18899delinsCAAT (CCNH)
NR_157069.2:n.1041-18902_1041-18899delinsCAAT (CCNH)
NR_157070.2:n.1205-18902_1205-18899delinsCAAT (CCNH)
NM_022650.3:c.161+194_161+197delinsATTG (RASA1)	NP_072179.1:n.161+194_161+197delinsATTG