Canonical Allele Identifier: CA351124446

Gene: SERPINE2

Linked Data

• MyVariant Identifiers: chr2:g.224862883G>A (hg19) ; chr2:g.223998166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998166G>A , CM000664.2:g.223998166G>A	GRCh38
NC_000002.11:g.224862883G>A , CM000664.1:g.224862883G>A	GRCh37
NC_000002.10:g.224571127G>A	NCBI36
NG_032907.1:g.46154C>T
NG_032907.2:g.46154C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.436C>T	ENSP00000258405.4:p.Pro146Ser
ENST00000409304.6:c.436C>T MANE Select	ENSP00000386412.1:p.Pro146Ser
ENST00000258405.8:c.436C>T	ENSP00000258405.4:p.Pro146Ser
ENST00000409304.5:c.436C>T	ENSP00000386412.1:p.Pro146Ser
ENST00000409840.7:c.436C>T	ENSP00000386969.3:p.Pro146Ser
ENST00000432738.5:c.436C>T	ENSP00000408452.1:p.Pro146Ser
ENST00000447280.6:c.472C>T	ENSP00000415786.2:p.Pro158Ser
NM_001136528.1:c.436C>T	NP_001130000.1:p.Pro146Ser
NM_001136530.1:c.472C>T	NP_001130002.1:p.Pro158Ser
NM_006216.3:c.436C>T	NP_006207.1:p.Pro146Ser
NR_073116.1:n.1097C>T
XM_005246641.2:c.472C>T	XP_005246698.1:p.Pro158Ser
XM_005246642.2:c.436C>T	XP_005246699.1:p.Pro146Ser
XM_017004330.1:c.436C>T	XP_016859819.1:p.Pro146Ser
XM_017004332.2:c.436C>T	XP_016859821.1:p.Pro146Ser
NM_001136528.2:c.436C>T MANE Select	NP_001130000.1:p.Pro146Ser
NM_006216.4:c.436C>T	NP_006207.1:p.Pro146Ser
NR_073116.2:n.1097C>T