Canonical Allele Identifier: CA540311895
Gene: SERPINE2 HGNC NCBI

Linked Data

dbSNP Id: rs1559204225

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223998118del , CM000664.2:g.223998118del GRCh38
NC_000002.11:g.224862835del , CM000664.1:g.224862835del GRCh37
NC_000002.10:g.224571079del NCBI36
NG_032907.1:g.46202del
NG_032907.2:g.46202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258405.9:c.484del ENSP00000258405.4:p.Arg162GlyfsTer3
ENST00000409304.6:c.484del MANE Select ENSP00000386412.1:p.Arg162GlyfsTer3
ENST00000258405.8:c.484del ENSP00000258405.4:p.Arg162GlyfsTer3
ENST00000409304.5:c.484del ENSP00000386412.1:p.Arg162GlyfsTer3
ENST00000409840.7:c.484del ENSP00000386969.3:p.Arg162GlyfsTer3
ENST00000432738.5:c.484del ENSP00000408452.1:p.Arg162GlyfsTer3
ENST00000447280.6:c.520del ENSP00000415786.2:p.Arg174GlyfsTer3
NM_001136528.1:c.484del NP_001130000.1:p.Arg162GlyfsTer3
NM_001136530.1:c.520del NP_001130002.1:p.Arg174GlyfsTer3
NM_006216.3:c.484del NP_006207.1:p.Arg162GlyfsTer3
NR_073116.1:n.1145del
XM_005246641.2:c.520del XP_005246698.1:p.Arg174GlyfsTer3
XM_005246642.2:c.484del XP_005246699.1:p.Arg162GlyfsTer3
XM_017004330.1:c.484del XP_016859819.1:p.Arg162GlyfsTer3
XM_017004332.2:c.484del XP_016859821.1:p.Arg162GlyfsTer3
NM_001136528.2:c.484del MANE Select NP_001130000.1:p.Arg162GlyfsTer3
NM_006216.4:c.484del NP_006207.1:p.Arg162GlyfsTer3
NR_073116.2:n.1145del