Canonical Allele Identifier: CA2578355194

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389574_87389575del , CM000667.2:g.87389574_87389575del	GRCh38
NC_000005.9:g.86685391_86685392del , CM000667.1:g.86685391_86685392del	GRCh37
NC_000005.8:g.86721147_86721148del	NCBI36
NG_011650.1:g.126241_126242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.3060+47_3060+48del (RASA1) MANE Select	ENSP00000274376.6:n.3060+47_3060+48del
ENST00000645953.1:c.*90+3197_*90+3198del (CCNH)	ENSP00000494460.1:n.*90+3197_*90+3198del
ENST00000646883.1:c.254+3197_254+3198del (CCNH)
ENST00000274376.10:c.3060+47_3060+48del (RASA1)	ENSP00000274376.6:n.3060+47_3060+48del
ENST00000456692.6:c.2529+47_2529+48del (RASA1)	ENSP00000411221.2:n.2529+47_2529+48del
ENST00000506290.1:c.2562+47_2562+48del (RASA1)	ENSP00000420905.1:n.2562+47_2562+48del
ENST00000512763.5:c.2559+47_2559+48del (RASA1)	ENSP00000422008.1:n.2559+47_2559+48del
ENST00000515800.6:c.*1675+47_*1675+48del (RASA1)	ENSP00000423395.2:n.*1675+47_*1675+48del
NM_002890.2:c.3060+47_3060+48del (RASA1)	NP_002881.1:n.3060+47_3060+48del
NM_022650.2:c.2529+47_2529+48del (RASA1)	NP_072179.1:n.2529+47_2529+48del
XM_011543525.1:c.2973+47_2973+48del (RASA1)	XP_011541827.1:n.2973+47_2973+48del
NM_001364075.1:c.933+5471_933+5472del (CCNH)	NP_001351004.1:n.933+5471_933+5472del
NR_157068.1:n.1447+3197_1447+3198del (CCNH)
NR_157069.1:n.1040+3197_1040+3198del (CCNH)
NR_157070.1:n.1204+3197_1204+3198del (CCNH)
XM_011543525.2:c.2973+47_2973+48del (RASA1)	XP_011541827.1:n.2973+47_2973+48del
NM_001364075.2:c.933+5471_933+5472del (CCNH)	NP_001351004.1:n.933+5471_933+5472del
NM_002890.3:c.3060+47_3060+48del (RASA1) MANE Select	NP_002881.1:n.3060+47_3060+48del
NR_157068.2:n.1447+3197_1447+3198del (CCNH)
NR_157069.2:n.1040+3197_1040+3198del (CCNH)
NR_157070.2:n.1204+3197_1204+3198del (CCNH)
NM_022650.3:c.2529+47_2529+48del (RASA1)	NP_072179.1:n.2529+47_2529+48del