Canonical Allele Identifier: CA1331326180

Gene: SERPINE2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998270G= , CM000664.2:g.223998270G=	GRCh38
NC_000002.11:g.224862987G= , CM000664.1:g.224862987G=	GRCh37
NC_000002.10:g.224571231G=	NCBI36
NG_032907.1:g.46050C=
NG_032907.2:g.46050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.332C=	ENSP00000258405.4:p.Ala111=
ENST00000409304.6:c.332C= MANE Select	ENSP00000386412.1:p.Ala111=
ENST00000258405.8:c.332C=	ENSP00000258405.4:p.Ala111=
ENST00000409304.5:c.332C=	ENSP00000386412.1:p.Ala111=
ENST00000409840.7:c.332C=	ENSP00000386969.3:p.Ala111=
ENST00000432738.5:c.332C=	ENSP00000408452.1:p.Ala111=
ENST00000447280.6:c.368C=	ENSP00000415786.2:p.Ala123=
NM_001136528.1:c.332C=	NP_001130000.1:p.Ala111=
NM_001136530.1:c.368C=	NP_001130002.1:p.Ala123=
NM_006216.3:c.332C=	NP_006207.1:p.Ala111=
NR_073116.1:n.993C=
XM_005246641.2:c.368C=	XP_005246698.1:p.Ala123=
XM_005246642.2:c.332C=	XP_005246699.1:p.Ala111=
XM_017004330.1:c.332C=	XP_016859819.1:p.Ala111=
XM_017004332.2:c.332C=	XP_016859821.1:p.Ala111=
NM_001136528.2:c.332C= MANE Select	NP_001130000.1:p.Ala111=
NM_006216.4:c.332C=	NP_006207.1:p.Ala111=
NR_073116.2:n.993C=