Canonical Allele Identifier: CA1561548498

Gene: RASA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87269040A= , CM000667.2:g.87269040A=	GRCh38
NC_000005.9:g.86564857A= , CM000667.1:g.86564857A=	GRCh37
NC_000005.8:g.86600613A=	NCBI36
NG_011650.1:g.5707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.539+50A= MANE Select	ENSP00000274376.6:n.539+50A=
ENST00000274376.10:c.539+50A=	ENSP00000274376.6:n.539+50A=
ENST00000456692.6:c.-8A=	ENSP00000411221.2:n.-8A=
ENST00000506290.1:c.-21A=	ENSP00000420905.1:n.-21A=
ENST00000512763.5:c.-105A=	ENSP00000422008.1:n.-105A=
ENST00000515800.6:c.539+50A=	ENSP00000423395.2:n.539+50A=
NM_002890.2:c.539+50A=	NP_002881.1:n.539+50A=
NM_022650.2:c.-8A=	NP_072179.1:n.-8A=
XM_011543525.1:c.539+50A=	XP_011541827.1:n.539+50A=
XM_011543526.1:c.539+50A=	XP_011541828.1:n.539+50A=
XM_011543527.1:c.539+50A=	XP_011541829.1:n.539+50A=
XM_011543525.2:c.539+50A=	XP_011541827.1:n.539+50A=
XM_011543527.3:c.539+50A=	XP_011541829.1:n.539+50A=
NM_002890.3:c.539+50A= MANE Select	NP_002881.1:n.539+50A=
NM_022650.3:c.-8A=	NP_072179.1:n.-8A=