Canonical Allele Identifier: CA1561615400

Gene: RASA1 CCNH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87389351A= , CM000667.2:g.87389351A=	GRCh38
NC_000005.9:g.86685168A= , CM000667.1:g.86685168A=	GRCh37
NC_000005.8:g.86720924A=	NCBI36
NG_011650.1:g.126018A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.2926-42A= (RASA1) MANE Select	ENSP00000274376.6:n.2926-42A=
ENST00000645953.1:c.*90+3419T= (CCNH)	ENSP00000494460.1:n.*90+3419T=
ENST00000646883.1:c.254+3419T= (CCNH)
ENST00000274376.10:c.2926-42A= (RASA1)	ENSP00000274376.6:n.2926-42A=
ENST00000456692.6:c.2395-42A= (RASA1)	ENSP00000411221.2:n.2395-42A=
ENST00000506290.1:c.2428-42A= (RASA1)	ENSP00000420905.1:n.2428-42A=
ENST00000512763.5:c.2425-42A= (RASA1)	ENSP00000422008.1:n.2425-42A=
ENST00000515800.6:c.*1499A= (RASA1)	ENSP00000423395.2:n.*1499A=
NM_002890.2:c.2926-42A= (RASA1)	NP_002881.1:n.2926-42A=
NM_022650.2:c.2395-42A= (RASA1)	NP_072179.1:n.2395-42A=
XM_011543525.1:c.2839-42A= (RASA1)	XP_011541827.1:n.2839-42A=
NM_001364075.1:c.933+5693T= (CCNH)	NP_001351004.1:n.933+5693T=
NR_157068.1:n.1447+3419T= (CCNH)
NR_157069.1:n.1040+3419T= (CCNH)
NR_157070.1:n.1204+3419T= (CCNH)
XM_011543525.2:c.2839-42A= (RASA1)	XP_011541827.1:n.2839-42A=
NM_001364075.2:c.933+5693T= (CCNH)	NP_001351004.1:n.933+5693T=
NM_002890.3:c.2926-42A= (RASA1) MANE Select	NP_002881.1:n.2926-42A=
NR_157068.2:n.1447+3419T= (CCNH)
NR_157069.2:n.1040+3419T= (CCNH)
NR_157070.2:n.1204+3419T= (CCNH)
NM_022650.3:c.2395-42A= (RASA1)	NP_072179.1:n.2395-42A=