Canonical Allele Identifier: CA8274439

Gene: SERPINF2

Linked Data

• dbSNP Id: rs755865141
• ExAC: 17:1657681 G / A
• gnomAD v2: 17-1657681-G-A
• gnomAD v4: 17-1754387-G-A
• MyVariant Identifiers: chr17:g.1657681G>A (hg19) ; chr17:g.1754387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754387G>A , CM000679.2:g.1754387G>A	GRCh38
NC_000017.10:g.1657681G>A , CM000679.1:g.1657681G>A	GRCh37
NC_000017.9:g.1604431G>A	NCBI36
NG_013215.1:g.16552G>A , LRG_885:g.16552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1329G>A	ENSP00000371493.4:p.Glu443=
ENST00000453066.6:c.1329G>A MANE Select	ENSP00000402286.2:p.Glu443=
ENST00000324015.7:c.1329G>A	ENSP00000321853.3:p.Glu443=
ENST00000382061.4:c.1329G>A	ENSP00000371493.4:p.Glu443=
ENST00000450523.6:c.1137G>A	ENSP00000403877.2:p.Glu379=
NM_000934.3:c.1329G>A , LRG_885t1:c.1329G>A	NP_000925.2:p.Glu443=
NM_001165920.1:c.1329G>A	NP_001159392.1:p.Glu443=
NM_001165921.1:c.1137G>A	NP_001159393.1:p.Glu379=
XM_005256699.3:c.1434G>A	XP_005256756.1:p.Glu478=
XM_005256700.3:c.1341G>A	XP_005256757.1:p.Glu447=
XM_005256701.3:c.1377G>A	XP_005256758.2:p.Glu459=
XM_005256703.3:c.1248G>A	XP_005256760.1:p.Glu416=
XM_005256701.4:c.1377G>A	XP_005256758.2:p.Glu459=
XM_017024765.1:c.1341G>A	XP_016880254.1:p.Glu447=
XM_024450805.1:c.1341G>A	XP_024306573.1:p.Glu447=
NM_000934.4:c.1329G>A MANE Select	NP_000925.2:p.Glu443=
NM_001165921.2:c.1137G>A	NP_001159393.1:p.Glu379=