Canonical Allele Identifier: CA351124313

Gene: SERPINE2

Linked Data

• gnomAD v4: 2-223998138-G-C
• MyVariant Identifiers: chr2:g.224862855G>C (hg19) ; chr2:g.223998138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.223998138G>C , CM000664.2:g.223998138G>C	GRCh38
NC_000002.11:g.224862855G>C , CM000664.1:g.224862855G>C	GRCh37
NC_000002.10:g.224571099G>C	NCBI36
NG_032907.1:g.46182C>G
NG_032907.2:g.46182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258405.9:c.464C>G	ENSP00000258405.4:p.Ala155Gly
ENST00000409304.6:c.464C>G MANE Select	ENSP00000386412.1:p.Ala155Gly
ENST00000258405.8:c.464C>G	ENSP00000258405.4:p.Ala155Gly
ENST00000409304.5:c.464C>G	ENSP00000386412.1:p.Ala155Gly
ENST00000409840.7:c.464C>G	ENSP00000386969.3:p.Ala155Gly
ENST00000432738.5:c.464C>G	ENSP00000408452.1:p.Ala155Gly
ENST00000447280.6:c.500C>G	ENSP00000415786.2:p.Ala167Gly
NM_001136528.1:c.464C>G	NP_001130000.1:p.Ala155Gly
NM_001136530.1:c.500C>G	NP_001130002.1:p.Ala167Gly
NM_006216.3:c.464C>G	NP_006207.1:p.Ala155Gly
NR_073116.1:n.1125C>G
XM_005246641.2:c.500C>G	XP_005246698.1:p.Ala167Gly
XM_005246642.2:c.464C>G	XP_005246699.1:p.Ala155Gly
XM_017004330.1:c.464C>G	XP_016859819.1:p.Ala155Gly
XM_017004332.2:c.464C>G	XP_016859821.1:p.Ala155Gly
NM_001136528.2:c.464C>G MANE Select	NP_001130000.1:p.Ala155Gly
NM_006216.4:c.464C>G	NP_006207.1:p.Ala155Gly
NR_073116.2:n.1125C>G