Canonical Allele Identifier: CA1331316876

Gene: SERPINE2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223977278C= , CM000664.2:g.223977278C=	GRCh38
NC_000002.11:g.224841995C= , CM000664.1:g.224841995C=	GRCh37
NC_000002.10:g.224550239C=	NCBI36
NG_032907.1:g.67042G=
NG_032907.2:g.67042G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.1159+266G=	ENSP00000258405.4:n.1159+266G=
ENST00000409304.6:c.1156+266G= MANE Select	ENSP00000386412.1:n.1156+266G=
ENST00000258405.8:c.1159+266G=	ENSP00000258405.4:n.1159+266G=
ENST00000409304.5:c.1156+266G=	ENSP00000386412.1:n.1156+266G=
ENST00000409840.7:c.1156+266G=	ENSP00000386969.3:n.1156+266G=
ENST00000447280.6:c.1192+266G=	ENSP00000415786.2:n.1192+266G=
ENST00000473202.1:n.5237+266G=
ENST00000478966.1:n.589+266G=
NM_001136528.1:c.1156+266G=	NP_001130000.1:n.1156+266G=
NM_001136530.1:c.1192+266G=	NP_001130002.1:n.1192+266G=
NM_006216.3:c.1159+266G=	NP_006207.1:n.1159+266G=
NR_073116.1:n.1817+266G=
XM_005246641.2:c.1195+266G=	XP_005246698.1:n.1195+266G=
XM_005246642.2:c.1159+266G=	XP_005246699.1:n.1159+266G=
XM_017004330.1:c.1159+266G=	XP_016859819.1:n.1159+266G=
XM_017004332.2:c.1156+266G=	XP_016859821.1:n.1156+266G=
NM_001136528.2:c.1156+266G= MANE Select	NP_001130000.1:n.1156+266G=
NM_006216.4:c.1159+266G=	NP_006207.1:n.1159+266G=
NR_073116.2:n.1817+266G=