Canonical Allele Identifier: CA2243019073

Gene: SERPINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754325A= , CM000679.2:g.1754325A=	GRCh38
NC_000017.10:g.1657619A= , CM000679.1:g.1657619A=	GRCh37
NC_000017.9:g.1604369A=	NCBI36
NG_013215.1:g.16490A= , LRG_885:g.16490A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1267A=	ENSP00000371493.4:p.Thr423=
ENST00000453066.6:c.1267A= MANE Select	ENSP00000402286.2:p.Thr423=
ENST00000324015.7:c.1267A=	ENSP00000321853.3:p.Thr423=
ENST00000382061.4:c.1267A=	ENSP00000371493.4:p.Thr423=
ENST00000450523.6:c.1075A=	ENSP00000403877.2:p.Thr359=
NM_000934.3:c.1267A= , LRG_885t1:c.1267A=	NP_000925.2:p.Thr423=
NM_001165920.1:c.1267A=	NP_001159392.1:p.Thr423=
NM_001165921.1:c.1075A=	NP_001159393.1:p.Thr359=
XM_005256699.3:c.1372A=	XP_005256756.1:p.Thr458=
XM_005256700.3:c.1279A=	XP_005256757.1:p.Thr427=
XM_005256701.3:c.1315A=	XP_005256758.2:p.Thr439=
XM_005256703.3:c.1186A=	XP_005256760.1:p.Thr396=
XM_005256701.4:c.1315A=	XP_005256758.2:p.Thr439=
XM_017024765.1:c.1279A=	XP_016880254.1:p.Thr427=
XM_024450805.1:c.1279A=	XP_024306573.1:p.Thr427=
NM_000934.4:c.1267A= MANE Select	NP_000925.2:p.Thr423=
NM_001165921.2:c.1075A=	NP_001159393.1:p.Thr359=