Canonical Allele Identifier: CA351124286

Gene: SERPINE2

Linked Data

• MyVariant Identifiers: chr2:g.224862849A>T (hg19) ; chr2:g.223998132A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998132A>T , CM000664.2:g.223998132A>T	GRCh38
NC_000002.11:g.224862849A>T , CM000664.1:g.224862849A>T	GRCh37
NC_000002.10:g.224571093A>T	NCBI36
NG_032907.1:g.46188T>A
NG_032907.2:g.46188T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.470T>A	ENSP00000258405.4:p.Val157Asp
ENST00000409304.6:c.470T>A MANE Select	ENSP00000386412.1:p.Val157Asp
ENST00000258405.8:c.470T>A	ENSP00000258405.4:p.Val157Asp
ENST00000409304.5:c.470T>A	ENSP00000386412.1:p.Val157Asp
ENST00000409840.7:c.470T>A	ENSP00000386969.3:p.Val157Asp
ENST00000432738.5:c.470T>A	ENSP00000408452.1:p.Val157Asp
ENST00000447280.6:c.506T>A	ENSP00000415786.2:p.Val169Asp
NM_001136528.1:c.470T>A	NP_001130000.1:p.Val157Asp
NM_001136530.1:c.506T>A	NP_001130002.1:p.Val169Asp
NM_006216.3:c.470T>A	NP_006207.1:p.Val157Asp
NR_073116.1:n.1131T>A
XM_005246641.2:c.506T>A	XP_005246698.1:p.Val169Asp
XM_005246642.2:c.470T>A	XP_005246699.1:p.Val157Asp
XM_017004330.1:c.470T>A	XP_016859819.1:p.Val157Asp
XM_017004332.2:c.470T>A	XP_016859821.1:p.Val157Asp
NM_001136528.2:c.470T>A MANE Select	NP_001130000.1:p.Val157Asp
NM_006216.4:c.470T>A	NP_006207.1:p.Val157Asp
NR_073116.2:n.1131T>A