Canonical Allele Identifier: CA2577259866

Gene: SERPINE2

Linked Data

• gnomAD v4: 2-223998081-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998083_223998084del , CM000664.2:g.223998083_223998084del	GRCh38
NC_000002.11:g.224862800_224862801del , CM000664.1:g.224862800_224862801del	GRCh37
NC_000002.10:g.224571044_224571045del	NCBI36
NG_032907.1:g.46237_46238del
NG_032907.2:g.46237_46238del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258405.9:c.487+32_487+33del	ENSP00000258405.4:n.487+32_487+33del
ENST00000409304.6:c.487+32_487+33del MANE Select	ENSP00000386412.1:n.487+32_487+33del
ENST00000258405.8:c.487+32_487+33del	ENSP00000258405.4:n.487+32_487+33del
ENST00000409304.5:c.487+32_487+33del	ENSP00000386412.1:n.487+32_487+33del
ENST00000409840.7:c.487+32_487+33del	ENSP00000386969.3:n.487+32_487+33del
ENST00000432738.5:c.487+32_487+33del	ENSP00000408452.1:n.487+32_487+33del
ENST00000447280.6:c.523+32_523+33del	ENSP00000415786.2:n.523+32_523+33del
NM_001136528.1:c.487+32_487+33del	NP_001130000.1:n.487+32_487+33del
NM_001136530.1:c.523+32_523+33del	NP_001130002.1:n.523+32_523+33del
NM_006216.3:c.487+32_487+33del	NP_006207.1:n.487+32_487+33del
NR_073116.1:n.1148+32_1148+33del
XM_005246641.2:c.523+32_523+33del	XP_005246698.1:n.523+32_523+33del
XM_005246642.2:c.487+32_487+33del	XP_005246699.1:n.487+32_487+33del
XM_017004330.1:c.487+32_487+33del	XP_016859819.1:n.487+32_487+33del
XM_017004332.2:c.487+32_487+33del	XP_016859821.1:n.487+32_487+33del
NM_001136528.2:c.487+32_487+33del MANE Select	NP_001130000.1:n.487+32_487+33del
NM_006216.4:c.487+32_487+33del	NP_006207.1:n.487+32_487+33del
NR_073116.2:n.1148+32_1148+33del