Canonical Allele Identifier: CA1561548507

Gene: RASA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.87269049T= , CM000667.2:g.87269049T=	GRCh38
NC_000005.9:g.86564866T= , CM000667.1:g.86564866T=	GRCh37
NC_000005.8:g.86600622T=	NCBI36
NG_011650.1:g.5716T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274376.11:c.539+59T= MANE Select	ENSP00000274376.6:n.539+59T=
ENST00000274376.10:c.539+59T=	ENSP00000274376.6:n.539+59T=
ENST00000456692.6:c.2T=	ENSP00000411221.2:p.Met1=
ENST00000506290.1:c.-12T=	ENSP00000420905.1:n.-12T=
ENST00000512763.5:c.-96T=	ENSP00000422008.1:n.-96T=
ENST00000515800.6:c.539+59T=	ENSP00000423395.2:n.539+59T=
NM_002890.2:c.539+59T=	NP_002881.1:n.539+59T=
NM_022650.2:c.2T=	NP_072179.1:p.Met1=
XM_011543525.1:c.539+59T=	XP_011541827.1:n.539+59T=
XM_011543526.1:c.539+59T=	XP_011541828.1:n.539+59T=
XM_011543527.1:c.539+59T=	XP_011541829.1:n.539+59T=
XM_011543525.2:c.539+59T=	XP_011541827.1:n.539+59T=
XM_011543527.3:c.539+59T=	XP_011541829.1:n.539+59T=
NM_002890.3:c.539+59T= MANE Select	NP_002881.1:n.539+59T=
NM_022650.3:c.2T=	NP_072179.1:p.Met1=