Canonical Allele Identifier: CA2767339850

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87385663_87385664insCTGGACCTTGAAAAATTCG , CM000667.2:g.87385663_87385664insCTGGACCTTGAAAAATTCG	GRCh38
NC_000005.9:g.86681480_86681481insCTGGACCTTGAAAAATTCG , CM000667.1:g.86681480_86681481insCTGGACCTTGAAAAATTCG	GRCh37
NC_000005.8:g.86717236_86717237insCTGGACCTTGAAAAATTCG	NCBI36
NG_011650.1:g.122330_122331insCTGGACCTTGAAAAATTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2847+274_2847+275insCTGGACCTTGAAAAATTCG (RASA1) MANE Select	ENSP00000274376.6:n.2847+274_2847+275insCTGGACCTTGAAAAATTCG
ENST00000645953.1:c.*90+7106_*90+7107insCGAATTTTTCAAGGTCCAG (CCNH)	ENSP00000494460.1:n.*90+7106_*90+7107insCGAATTTTTCAAGGTCCAG
ENST00000646883.1:c.254+7106_254+7107insCGAATTTTTCAAGGTCCAG (CCNH)
ENST00000274376.10:c.2847+274_2847+275insCTGGACCTTGAAAAATTCG (RASA1)	ENSP00000274376.6:n.2847+274_2847+275insCTGGACCTTGAAAAATTCG
ENST00000456692.6:c.2316+274_2316+275insCTGGACCTTGAAAAATTCG (RASA1)	ENSP00000411221.2:n.2316+274_2316+275insCTGGACCTTGAAAAATTCG
ENST00000506290.1:c.2349+274_2349+275insCTGGACCTTGAAAAATTCG (RASA1)	ENSP00000420905.1:n.2349+274_2349+275insCTGGACCTTGAAAAATTCG
ENST00000512763.5:c.2346+274_2346+275insCTGGACCTTGAAAAATTCG (RASA1)	ENSP00000422008.1:n.2346+274_2346+275insCTGGACCTTGAAAAATTCG
ENST00000515800.6:c.*1372+274_*1372+275insCTGGACCTTGAAAAATTCG (RASA1)	ENSP00000423395.2:n.*1372+274_*1372+275insCTGGACCTTGAAAAATTCG...
NM_002890.2:c.2847+274_2847+275insCTGGACCTTGAAAAATTCG (RASA1)	NP_002881.1:n.2847+274_2847+275insCTGGACCTTGAAAAATTCG
NM_022650.2:c.2316+274_2316+275insCTGGACCTTGAAAAATTCG (RASA1)	NP_072179.1:n.2316+274_2316+275insCTGGACCTTGAAAAATTCG
XM_011543525.1:c.2760+274_2760+275insCTGGACCTTGAAAAATTCG (RASA1)	XP_011541827.1:n.2760+274_2760+275insCTGGACCTTGAAAAATTCG
XM_011543526.1:c.2847+274_2847+275insCTGGACCTTGAAAAATTCG (RASA1)	XP_011541828.1:n.2847+274_2847+275insCTGGACCTTGAAAAATTCG
NM_001364075.1:c.933+9380_933+9381insCGAATTTTTCAAGGTCCAG (CCNH)	NP_001351004.1:n.933+9380_933+9381insCGAATTTTTCAAGGTCCAG
NR_157068.1:n.1447+7106_1447+7107insCGAATTTTTCAAGGTCCAG (CCNH)
NR_157069.1:n.1040+7106_1040+7107insCGAATTTTTCAAGGTCCAG (CCNH)
NR_157070.1:n.1204+7106_1204+7107insCGAATTTTTCAAGGTCCAG (CCNH)
XM_011543525.2:c.2760+274_2760+275insCTGGACCTTGAAAAATTCG (RASA1)	XP_011541827.1:n.2760+274_2760+275insCTGGACCTTGAAAAATTCG
NM_001364075.2:c.933+9380_933+9381insCGAATTTTTCAAGGTCCAG (CCNH)	NP_001351004.1:n.933+9380_933+9381insCGAATTTTTCAAGGTCCAG
NM_002890.3:c.2847+274_2847+275insCTGGACCTTGAAAAATTCG (RASA1) MANE Select	NP_002881.1:n.2847+274_2847+275insCTGGACCTTGAAAAATTCG
NR_157068.2:n.1447+7106_1447+7107insCGAATTTTTCAAGGTCCAG (CCNH)
NR_157069.2:n.1040+7106_1040+7107insCGAATTTTTCAAGGTCCAG (CCNH)
NR_157070.2:n.1204+7106_1204+7107insCGAATTTTTCAAGGTCCAG (CCNH)
NM_022650.3:c.2316+274_2316+275insCTGGACCTTGAAAAATTCG (RASA1)	NP_072179.1:n.2316+274_2316+275insCTGGACCTTGAAAAATTCG