Canonical Allele Identifier: CA1331326038

Gene: SERPINE2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223997943C= , CM000664.2:g.223997943C=	GRCh38
NC_000002.11:g.224862660C= , CM000664.1:g.224862660C=	GRCh37
NC_000002.10:g.224570904C=	NCBI36
NG_032907.1:g.46377G=
NG_032907.2:g.46377G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.487+172G=	ENSP00000258405.4:n.487+172G=
ENST00000409304.6:c.487+172G= MANE Select	ENSP00000386412.1:n.487+172G=
ENST00000258405.8:c.487+172G=	ENSP00000258405.4:n.487+172G=
ENST00000409304.5:c.487+172G=	ENSP00000386412.1:n.487+172G=
ENST00000409840.7:c.487+172G=	ENSP00000386969.3:n.487+172G=
ENST00000432738.5:c.487+172G=	ENSP00000408452.1:n.487+172G=
ENST00000447280.6:c.523+172G=	ENSP00000415786.2:n.523+172G=
NM_001136528.1:c.487+172G=	NP_001130000.1:n.487+172G=
NM_001136530.1:c.523+172G=	NP_001130002.1:n.523+172G=
NM_006216.3:c.487+172G=	NP_006207.1:n.487+172G=
NR_073116.1:n.1148+172G=
XM_005246641.2:c.523+172G=	XP_005246698.1:n.523+172G=
XM_005246642.2:c.487+172G=	XP_005246699.1:n.487+172G=
XM_017004330.1:c.487+172G=	XP_016859819.1:n.487+172G=
XM_017004332.2:c.487+172G=	XP_016859821.1:n.487+172G=
NM_001136528.2:c.487+172G= MANE Select	NP_001130000.1:n.487+172G=
NM_006216.4:c.487+172G=	NP_006207.1:n.487+172G=
NR_073116.2:n.1148+172G=