Canonical Allele Identifier: CA2663362747
Gene: SERPINE2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223997976_223997983del , CM000664.2:g.223997976_223997983del GRCh38
NC_000002.11:g.224862693_224862700del , CM000664.1:g.224862693_224862700del GRCh37
NC_000002.10:g.224570937_224570944del NCBI36
NG_032907.1:g.46337_46344del
NG_032907.2:g.46337_46344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258405.9:c.487+132_487+139del ENSP00000258405.4:n.487+132_487+139del
ENST00000409304.6:c.487+132_487+139del MANE Select ENSP00000386412.1:n.487+132_487+139del
ENST00000258405.8:c.487+132_487+139del ENSP00000258405.4:n.487+132_487+139del
ENST00000409304.5:c.487+132_487+139del ENSP00000386412.1:n.487+132_487+139del
ENST00000409840.7:c.487+132_487+139del ENSP00000386969.3:n.487+132_487+139del
ENST00000432738.5:c.487+132_487+139del ENSP00000408452.1:n.487+132_487+139del
ENST00000447280.6:c.523+132_523+139del ENSP00000415786.2:n.523+132_523+139del
NM_001136528.1:c.487+132_487+139del NP_001130000.1:n.487+132_487+139del
NM_001136530.1:c.523+132_523+139del NP_001130002.1:n.523+132_523+139del
NM_006216.3:c.487+132_487+139del NP_006207.1:n.487+132_487+139del
NR_073116.1:n.1148+132_1148+139del
XM_005246641.2:c.523+132_523+139del XP_005246698.1:n.523+132_523+139del
XM_005246642.2:c.487+132_487+139del XP_005246699.1:n.487+132_487+139del
XM_017004330.1:c.487+132_487+139del XP_016859819.1:n.487+132_487+139del
XM_017004332.2:c.487+132_487+139del XP_016859821.1:n.487+132_487+139del
NM_001136528.2:c.487+132_487+139del MANE Select NP_001130000.1:n.487+132_487+139del
NM_006216.4:c.487+132_487+139del NP_006207.1:n.487+132_487+139del
NR_073116.2:n.1148+132_1148+139del