Canonical Allele Identifier: CA1561548446

Gene: RASA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87269028G= , CM000667.2:g.87269028G=	GRCh38
NC_000005.9:g.86564845G= , CM000667.1:g.86564845G=	GRCh37
NC_000005.8:g.86600601G=	NCBI36
NG_011650.1:g.5695G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.539+38G= MANE Select	ENSP00000274376.6:n.539+38G=
ENST00000274376.10:c.539+38G=	ENSP00000274376.6:n.539+38G=
ENST00000456692.6:c.-20G=	ENSP00000411221.2:n.-20G=
ENST00000506290.1:c.-33G=	ENSP00000420905.1:n.-33G=
ENST00000512763.5:c.-117G=	ENSP00000422008.1:n.-117G=
ENST00000515800.6:c.539+38G=	ENSP00000423395.2:n.539+38G=
NM_002890.2:c.539+38G=	NP_002881.1:n.539+38G=
NM_022650.2:c.-20G=	NP_072179.1:n.-20G=
XM_011543525.1:c.539+38G=	XP_011541827.1:n.539+38G=
XM_011543526.1:c.539+38G=	XP_011541828.1:n.539+38G=
XM_011543527.1:c.539+38G=	XP_011541829.1:n.539+38G=
XM_011543525.2:c.539+38G=	XP_011541827.1:n.539+38G=
XM_011543527.3:c.539+38G=	XP_011541829.1:n.539+38G=
NM_002890.3:c.539+38G= MANE Select	NP_002881.1:n.539+38G=
NM_022650.3:c.-20G=	NP_072179.1:n.-20G=