Canonical Allele Identifier: CA1561548425

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87363533_87363534delinsCG , CM000667.2:g.87363533_87363534delinsCG	GRCh38
NC_000005.9:g.86659350_86659351delinsCG , CM000667.1:g.86659350_86659351delinsCG	GRCh37
NC_000005.8:g.86695106_86695107delinsCG	NCBI36
NG_011650.1:g.100200_100201delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.1610+29_1610+30delinsCG (RASA1) MANE Select	ENSP00000274376.6:n.1610+29_1610+30delinsCG
ENST00000645953.1:c.*90+29236_*90+29237delinsCG (CCNH)	ENSP00000494460.1:n.*90+29236_*90+29237delinsCG
ENST00000274376.10:c.1610+29_1610+30delinsCG (RASA1)	ENSP00000274376.6:n.1610+29_1610+30delinsCG
ENST00000456692.6:c.1079+29_1079+30delinsCG (RASA1)	ENSP00000411221.2:n.1079+29_1079+30delinsCG
ENST00000506290.1:c.1112+29_1112+30delinsCG (RASA1)	ENSP00000420905.1:n.1112+29_1112+30delinsCG
ENST00000509953.1:n.713+29_713+30delinsCG (RASA1)
ENST00000512763.5:c.1109+29_1109+30delinsCG (RASA1)	ENSP00000422008.1:n.1109+29_1109+30delinsCG
ENST00000515800.6:c.1610+29_1610+30delinsCG (RASA1)	ENSP00000423395.2:n.1610+29_1610+30delinsCG
NM_002890.2:c.1610+29_1610+30delinsCG (RASA1)	NP_002881.1:n.1610+29_1610+30delinsCG
NM_022650.2:c.1079+29_1079+30delinsCG (RASA1)	NP_072179.1:n.1079+29_1079+30delinsCG
XM_011543525.1:c.1610+29_1610+30delinsCG (RASA1)	XP_011541827.1:n.1610+29_1610+30delinsCG
XM_011543526.1:c.1610+29_1610+30delinsCG (RASA1)	XP_011541828.1:n.1610+29_1610+30delinsCG
XM_011543527.1:c.1610+29_1610+30delinsCG (RASA1)	XP_011541829.1:n.1610+29_1610+30delinsCG
NM_001364075.1:c.933+31510_933+31511delinsCG (CCNH)	NP_001351004.1:n.933+31510_933+31511delinsCG
NR_157068.1:n.1447+29236_1447+29237delinsCG (CCNH)
NR_157069.1:n.1040+29236_1040+29237delinsCG (CCNH)
NR_157070.1:n.1204+29236_1204+29237delinsCG (CCNH)
XM_011543525.2:c.1610+29_1610+30delinsCG (RASA1)	XP_011541827.1:n.1610+29_1610+30delinsCG
XM_011543527.3:c.1610+29_1610+30delinsCG (RASA1)	XP_011541829.1:n.1610+29_1610+30delinsCG
NM_001364075.2:c.933+31510_933+31511delinsCG (CCNH)	NP_001351004.1:n.933+31510_933+31511delinsCG
NM_002890.3:c.1610+29_1610+30delinsCG (RASA1) MANE Select	NP_002881.1:n.1610+29_1610+30delinsCG
NR_157068.2:n.1447+29236_1447+29237delinsCG (CCNH)
NR_157069.2:n.1040+29236_1040+29237delinsCG (CCNH)
NR_157070.2:n.1204+29236_1204+29237delinsCG (CCNH)
NM_022650.3:c.1079+29_1079+30delinsCG (RASA1)	NP_072179.1:n.1079+29_1079+30delinsCG