Canonical Allele Identifier: CA2326773386

Gene: SUGP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19296909T= , CM000681.2:g.19296909T=	GRCh38
NC_000019.9:g.19407718T= , CM000681.1:g.19407718T=	GRCh37
NC_000019.8:g.19268718T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_172231.4:c.1243+80A= MANE Select	NP_757386.2:n.1243+80A=
ENST00000247001.10:c.1243+80A= MANE Select	ENSP00000247001.3:n.1243+80A=
NM_172231.3:c.1243+80A=	NP_757386.2:n.1243+80A=
ENST00000247001.9:c.1243+80A=	ENSP00000247001.3:n.1243+80A=
ENST00000587119.5:c.*945+80A=	ENSP00000466188.1:n.*945+80A=
ENST00000588731.6:c.*770+80A=	ENSP00000465413.2:n.*770+80A=
ENST00000589144.5:c.741+80A=
ENST00000591007.6:n.547+80A=
XM_005260002.1:c.613+80A=	XP_005260059.1:n.613+80A=
XM_005260002.3:c.613+80A=	XP_005260059.1:n.613+80A=
XM_011528155.1:c.613+80A=	XP_011526457.1:n.613+80A=
XM_011528155.2:c.613+80A=	XP_011526457.1:n.613+80A=
XM_024451627.1:c.712+80A=	XP_024307395.1:n.712+80A=
XM_024451628.1:c.613+80A=	XP_024307396.1:n.613+80A=