Canonical Allele Identifier: CA2577259857

Gene: SERPINE2

Linked Data

• gnomAD v4: 2-223998027-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998027G>C , CM000664.2:g.223998027G>C	GRCh38
NC_000002.11:g.224862744G>C , CM000664.1:g.224862744G>C	GRCh37
NC_000002.10:g.224570988G>C	NCBI36
NG_032907.1:g.46293C>G
NG_032907.2:g.46293C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258405.9:c.487+88C>G	ENSP00000258405.4:n.487+88C>G
ENST00000409304.6:c.487+88C>G MANE Select	ENSP00000386412.1:n.487+88C>G
ENST00000258405.8:c.487+88C>G	ENSP00000258405.4:n.487+88C>G
ENST00000409304.5:c.487+88C>G	ENSP00000386412.1:n.487+88C>G
ENST00000409840.7:c.487+88C>G	ENSP00000386969.3:n.487+88C>G
ENST00000432738.5:c.487+88C>G	ENSP00000408452.1:n.487+88C>G
ENST00000447280.6:c.523+88C>G	ENSP00000415786.2:n.523+88C>G
NM_001136528.1:c.487+88C>G	NP_001130000.1:n.487+88C>G
NM_001136530.1:c.523+88C>G	NP_001130002.1:n.523+88C>G
NM_006216.3:c.487+88C>G	NP_006207.1:n.487+88C>G
NR_073116.1:n.1148+88C>G
XM_005246641.2:c.523+88C>G	XP_005246698.1:n.523+88C>G
XM_005246642.2:c.487+88C>G	XP_005246699.1:n.487+88C>G
XM_017004330.1:c.487+88C>G	XP_016859819.1:n.487+88C>G
XM_017004332.2:c.487+88C>G	XP_016859821.1:n.487+88C>G
NM_001136528.2:c.487+88C>G MANE Select	NP_001130000.1:n.487+88C>G
NM_006216.4:c.487+88C>G	NP_006207.1:n.487+88C>G
NR_073116.2:n.1148+88C>G