Canonical Allele Identifier: CA1561548387

Gene: RASA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87268997T= , CM000667.2:g.87268997T=	GRCh38
NC_000005.9:g.86564814T= , CM000667.1:g.86564814T=	GRCh37
NC_000005.8:g.86600570T=	NCBI36
NG_011650.1:g.5664T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274376.11:c.539+7T= MANE Select	ENSP00000274376.6:n.539+7T=
ENST00000274376.10:c.539+7T=	ENSP00000274376.6:n.539+7T=
ENST00000456692.6:c.-51T=	ENSP00000411221.2:n.-51T=
ENST00000506290.1:c.-64T=	ENSP00000420905.1:n.-64T=
ENST00000512763.5:c.-148T=	ENSP00000422008.1:n.-148T=
ENST00000515800.6:c.539+7T=	ENSP00000423395.2:n.539+7T=
NM_002890.2:c.539+7T=	NP_002881.1:n.539+7T=
NM_022650.2:c.-51T=	NP_072179.1:n.-51T=
XM_011543525.1:c.539+7T=	XP_011541827.1:n.539+7T=
XM_011543526.1:c.539+7T=	XP_011541828.1:n.539+7T=
XM_011543527.1:c.539+7T=	XP_011541829.1:n.539+7T=
XM_011543525.2:c.539+7T=	XP_011541827.1:n.539+7T=
XM_011543527.3:c.539+7T=	XP_011541829.1:n.539+7T=
NM_002890.3:c.539+7T= MANE Select	NP_002881.1:n.539+7T=
NM_022650.3:c.-51T=	NP_072179.1:n.-51T=