Canonical Allele Identifier: CA1331326045

Gene: SERPINE2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223997959G= , CM000664.2:g.223997959G=	GRCh38
NC_000002.11:g.224862676G= , CM000664.1:g.224862676G=	GRCh37
NC_000002.10:g.224570920G=	NCBI36
NG_032907.1:g.46361C=
NG_032907.2:g.46361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.487+156C=	ENSP00000258405.4:n.487+156C=
ENST00000409304.6:c.487+156C= MANE Select	ENSP00000386412.1:n.487+156C=
ENST00000258405.8:c.487+156C=	ENSP00000258405.4:n.487+156C=
ENST00000409304.5:c.487+156C=	ENSP00000386412.1:n.487+156C=
ENST00000409840.7:c.487+156C=	ENSP00000386969.3:n.487+156C=
ENST00000432738.5:c.487+156C=	ENSP00000408452.1:n.487+156C=
ENST00000447280.6:c.523+156C=	ENSP00000415786.2:n.523+156C=
NM_001136528.1:c.487+156C=	NP_001130000.1:n.487+156C=
NM_001136530.1:c.523+156C=	NP_001130002.1:n.523+156C=
NM_006216.3:c.487+156C=	NP_006207.1:n.487+156C=
NR_073116.1:n.1148+156C=
XM_005246641.2:c.523+156C=	XP_005246698.1:n.523+156C=
XM_005246642.2:c.487+156C=	XP_005246699.1:n.487+156C=
XM_017004330.1:c.487+156C=	XP_016859819.1:n.487+156C=
XM_017004332.2:c.487+156C=	XP_016859821.1:n.487+156C=
NM_001136528.2:c.487+156C= MANE Select	NP_001130000.1:n.487+156C=
NM_006216.4:c.487+156C=	NP_006207.1:n.487+156C=
NR_073116.2:n.1148+156C=