Canonical Allele Identifier: CA397575790

Gene: SERPINF2

Linked Data

• gnomAD v4: 17-1754375-T-G
• MyVariant Identifiers: chr17:g.1657669T>G (hg19) ; chr17:g.1754375T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754375T>G , CM000679.2:g.1754375T>G	GRCh38
NC_000017.10:g.1657669T>G , CM000679.1:g.1657669T>G	GRCh37
NC_000017.9:g.1604419T>G	NCBI36
NG_013215.1:g.16540T>G , LRG_885:g.16540T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1317T>G	ENSP00000371493.4:p.Ser439Arg
ENST00000453066.6:c.1317T>G MANE Select	ENSP00000402286.2:p.Ser439Arg
ENST00000324015.7:c.1317T>G	ENSP00000321853.3:p.Ser439Arg
ENST00000382061.4:c.1317T>G	ENSP00000371493.4:p.Ser439Arg
ENST00000450523.6:c.1125T>G	ENSP00000403877.2:p.Ser375Arg
NM_000934.3:c.1317T>G , LRG_885t1:c.1317T>G	NP_000925.2:p.Ser439Arg
NM_001165920.1:c.1317T>G	NP_001159392.1:p.Ser439Arg
NM_001165921.1:c.1125T>G	NP_001159393.1:p.Ser375Arg
XM_005256699.3:c.1422T>G	XP_005256756.1:p.Ser474Arg
XM_005256700.3:c.1329T>G	XP_005256757.1:p.Ser443Arg
XM_005256701.3:c.1365T>G	XP_005256758.2:p.Ser455Arg
XM_005256703.3:c.1236T>G	XP_005256760.1:p.Ser412Arg
XM_005256701.4:c.1365T>G	XP_005256758.2:p.Ser455Arg
XM_017024765.1:c.1329T>G	XP_016880254.1:p.Ser443Arg
XM_024450805.1:c.1329T>G	XP_024306573.1:p.Ser443Arg
NM_000934.4:c.1317T>G MANE Select	NP_000925.2:p.Ser439Arg
NM_001165921.2:c.1125T>G	NP_001159393.1:p.Ser375Arg