Canonical Allele Identifier: CA1331326140

Gene: SERPINE2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998167A= , CM000664.2:g.223998167A=	GRCh38
NC_000002.11:g.224862884A= , CM000664.1:g.224862884A=	GRCh37
NC_000002.10:g.224571128A=	NCBI36
NG_032907.1:g.46153T=
NG_032907.2:g.46153T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.435T=	ENSP00000258405.4:p.Asp145=
ENST00000409304.6:c.435T= MANE Select	ENSP00000386412.1:p.Asp145=
ENST00000258405.8:c.435T=	ENSP00000258405.4:p.Asp145=
ENST00000409304.5:c.435T=	ENSP00000386412.1:p.Asp145=
ENST00000409840.7:c.435T=	ENSP00000386969.3:p.Asp145=
ENST00000432738.5:c.435T=	ENSP00000408452.1:p.Asp145=
ENST00000447280.6:c.471T=	ENSP00000415786.2:p.Asp157=
NM_001136528.1:c.435T=	NP_001130000.1:p.Asp145=
NM_001136530.1:c.471T=	NP_001130002.1:p.Asp157=
NM_006216.3:c.435T=	NP_006207.1:p.Asp145=
NR_073116.1:n.1096T=
XM_005246641.2:c.471T=	XP_005246698.1:p.Asp157=
XM_005246642.2:c.435T=	XP_005246699.1:p.Asp145=
XM_017004330.1:c.435T=	XP_016859819.1:p.Asp145=
XM_017004332.2:c.435T=	XP_016859821.1:p.Asp145=
NM_001136528.2:c.435T= MANE Select	NP_001130000.1:p.Asp145=
NM_006216.4:c.435T=	NP_006207.1:p.Asp145=
NR_073116.2:n.1096T=