Canonical Allele Identifier: CA1561608570

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87385576_87385578delinsAAC , CM000667.2:g.87385576_87385578delinsAAC	GRCh38
NC_000005.9:g.86681393_86681395delinsAAC , CM000667.1:g.86681393_86681395delinsAAC	GRCh37
NC_000005.8:g.86717149_86717151delinsAAC	NCBI36
NG_011650.1:g.122243_122245delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2847+187_2847+189delinsAAC (RASA1) MANE Select	ENSP00000274376.6:n.2847+187_2847+189delinsAAC
ENST00000645953.1:c.*90+7192_*90+7194delinsGTT (CCNH)	ENSP00000494460.1:n.*90+7192_*90+7194delinsGTT
ENST00000646883.1:c.254+7192_254+7194delinsGTT (CCNH)
ENST00000274376.10:c.2847+187_2847+189delinsAAC (RASA1)	ENSP00000274376.6:n.2847+187_2847+189delinsAAC
ENST00000456692.6:c.2316+187_2316+189delinsAAC (RASA1)	ENSP00000411221.2:n.2316+187_2316+189delinsAAC
ENST00000506290.1:c.2349+187_2349+189delinsAAC (RASA1)	ENSP00000420905.1:n.2349+187_2349+189delinsAAC
ENST00000512763.5:c.2346+187_2346+189delinsAAC (RASA1)	ENSP00000422008.1:n.2346+187_2346+189delinsAAC
ENST00000515800.6:c.*1372+187_*1372+189delinsAAC (RASA1)	ENSP00000423395.2:n.*1372+187_*1372+189delinsAAC
NM_002890.2:c.2847+187_2847+189delinsAAC (RASA1)	NP_002881.1:n.2847+187_2847+189delinsAAC
NM_022650.2:c.2316+187_2316+189delinsAAC (RASA1)	NP_072179.1:n.2316+187_2316+189delinsAAC
XM_011543525.1:c.2760+187_2760+189delinsAAC (RASA1)	XP_011541827.1:n.2760+187_2760+189delinsAAC
XM_011543526.1:c.2847+187_2847+189delinsAAC (RASA1)	XP_011541828.1:n.2847+187_2847+189delinsAAC
NM_001364075.1:c.933+9466_933+9468delinsGTT (CCNH)	NP_001351004.1:n.933+9466_933+9468delinsGTT
NR_157068.1:n.1447+7192_1447+7194delinsGTT (CCNH)
NR_157069.1:n.1040+7192_1040+7194delinsGTT (CCNH)
NR_157070.1:n.1204+7192_1204+7194delinsGTT (CCNH)
XM_011543525.2:c.2760+187_2760+189delinsAAC (RASA1)	XP_011541827.1:n.2760+187_2760+189delinsAAC
NM_001364075.2:c.933+9466_933+9468delinsGTT (CCNH)	NP_001351004.1:n.933+9466_933+9468delinsGTT
NM_002890.3:c.2847+187_2847+189delinsAAC (RASA1) MANE Select	NP_002881.1:n.2847+187_2847+189delinsAAC
NR_157068.2:n.1447+7192_1447+7194delinsGTT (CCNH)
NR_157069.2:n.1040+7192_1040+7194delinsGTT (CCNH)
NR_157070.2:n.1204+7192_1204+7194delinsGTT (CCNH)
NM_022650.3:c.2316+187_2316+189delinsAAC (RASA1)	NP_072179.1:n.2316+187_2316+189delinsAAC