Canonical Allele Identifier: CA1561579297

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87331649_87331653delinsTAGAG , CM000667.2:g.87331649_87331653delinsTAGAG	GRCh38
NC_000005.9:g.86627466_86627470delinsTAGAG , CM000667.1:g.86627466_86627470delinsTAGAG	GRCh37
NC_000005.8:g.86663222_86663226delinsTAGAG	NCBI36
NG_011650.1:g.68316_68320delinsTAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.692+149_692+153delinsTAGAG (RASA1) MANE Select	ENSP00000274376.6:n.692+149_692+153delinsTAGAG
ENST00000645953.1:c.*91-12756_*91-12752delinsCTCTA (CCNH)	ENSP00000494460.1:n.*91-12756_*91-12752delinsCTCTA
ENST00000274376.10:c.692+149_692+153delinsTAGAG (RASA1)	ENSP00000274376.6:n.692+149_692+153delinsTAGAG
ENST00000456692.6:c.161+149_161+153delinsTAGAG (RASA1)	ENSP00000411221.2:n.161+149_161+153delinsTAGAG
ENST00000506290.1:c.194+149_194+153delinsTAGAG (RASA1)	ENSP00000420905.1:n.194+149_194+153delinsTAGAG
ENST00000512763.5:c.191+149_191+153delinsTAGAG (RASA1)	ENSP00000422008.1:n.191+149_191+153delinsTAGAG
ENST00000515800.6:c.692+149_692+153delinsTAGAG (RASA1)	ENSP00000423395.2:n.692+149_692+153delinsTAGAG
NM_002890.2:c.692+149_692+153delinsTAGAG (RASA1)	NP_002881.1:n.692+149_692+153delinsTAGAG
NM_022650.2:c.161+149_161+153delinsTAGAG (RASA1)	NP_072179.1:n.161+149_161+153delinsTAGAG
XM_011543525.1:c.692+149_692+153delinsTAGAG (RASA1)	XP_011541827.1:n.692+149_692+153delinsTAGAG
XM_011543526.1:c.692+149_692+153delinsTAGAG (RASA1)	XP_011541828.1:n.692+149_692+153delinsTAGAG
XM_011543527.1:c.692+149_692+153delinsTAGAG (RASA1)	XP_011541829.1:n.692+149_692+153delinsTAGAG
NM_001364075.1:c.934-18858_934-18854delinsCTCTA (CCNH)	NP_001351004.1:n.934-18858_934-18854delinsCTCTA
NR_157068.1:n.1448-18858_1448-18854delinsCTCTA (CCNH)
NR_157069.1:n.1041-18858_1041-18854delinsCTCTA (CCNH)
NR_157070.1:n.1205-18858_1205-18854delinsCTCTA (CCNH)
XM_011543525.2:c.692+149_692+153delinsTAGAG (RASA1)	XP_011541827.1:n.692+149_692+153delinsTAGAG
XM_011543527.3:c.692+149_692+153delinsTAGAG (RASA1)	XP_011541829.1:n.692+149_692+153delinsTAGAG
NM_001364075.2:c.934-18858_934-18854delinsCTCTA (CCNH)	NP_001351004.1:n.934-18858_934-18854delinsCTCTA
NM_002890.3:c.692+149_692+153delinsTAGAG (RASA1) MANE Select	NP_002881.1:n.692+149_692+153delinsTAGAG
NR_157068.2:n.1448-18858_1448-18854delinsCTCTA (CCNH)
NR_157069.2:n.1041-18858_1041-18854delinsCTCTA (CCNH)
NR_157070.2:n.1205-18858_1205-18854delinsCTCTA (CCNH)
NM_022650.3:c.161+149_161+153delinsTAGAG (RASA1)	NP_072179.1:n.161+149_161+153delinsTAGAG