Canonical Allele Identifier: CA351124584

Gene: SERPINE2

Linked Data

• COSMIC: COSM720531 ; COSM1149035
• MyVariant Identifiers: chr2:g.224862912C>T (hg19) ; chr2:g.223998195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998195C>T , CM000664.2:g.223998195C>T	GRCh38
NC_000002.11:g.224862912C>T , CM000664.1:g.224862912C>T	GRCh37
NC_000002.10:g.224571156C>T	NCBI36
NG_032907.1:g.46125G>A
NG_032907.2:g.46125G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.407G>A	ENSP00000258405.4:p.Cys136Tyr
ENST00000409304.6:c.407G>A MANE Select	ENSP00000386412.1:p.Cys136Tyr
ENST00000258405.8:c.407G>A	ENSP00000258405.4:p.Cys136Tyr
ENST00000409304.5:c.407G>A	ENSP00000386412.1:p.Cys136Tyr
ENST00000409840.7:c.407G>A	ENSP00000386969.3:p.Cys136Tyr
ENST00000432738.5:c.407G>A	ENSP00000408452.1:p.Cys136Tyr
ENST00000447280.6:c.443G>A	ENSP00000415786.2:p.Cys148Tyr
NM_001136528.1:c.407G>A	NP_001130000.1:p.Cys136Tyr
NM_001136530.1:c.443G>A	NP_001130002.1:p.Cys148Tyr
NM_006216.3:c.407G>A	NP_006207.1:p.Cys136Tyr
NR_073116.1:n.1068G>A
XM_005246641.2:c.443G>A	XP_005246698.1:p.Cys148Tyr
XM_005246642.2:c.407G>A	XP_005246699.1:p.Cys136Tyr
XM_017004330.1:c.407G>A	XP_016859819.1:p.Cys136Tyr
XM_017004332.2:c.407G>A	XP_016859821.1:p.Cys136Tyr
NM_001136528.2:c.407G>A MANE Select	NP_001130000.1:p.Cys136Tyr
NM_006216.4:c.407G>A	NP_006207.1:p.Cys136Tyr
NR_073116.2:n.1068G>A