Canonical Allele Identifier: CA2243019037

Gene: SERPINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754297C= , CM000679.2:g.1754297C=	GRCh38
NC_000017.10:g.1657591C= , CM000679.1:g.1657591C=	GRCh37
NC_000017.9:g.1604341C=	NCBI36
NG_013215.1:g.16462C= , LRG_885:g.16462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1239C=	ENSP00000371493.4:p.Arg413=
ENST00000453066.6:c.1239C= MANE Select	ENSP00000402286.2:p.Arg413=
ENST00000324015.7:c.1239C=	ENSP00000321853.3:p.Arg413=
ENST00000382061.4:c.1239C=	ENSP00000371493.4:p.Arg413=
ENST00000450523.6:c.1047C=	ENSP00000403877.2:p.Arg349=
NM_000934.3:c.1239C= , LRG_885t1:c.1239C=	NP_000925.2:p.Arg413=
NM_001165920.1:c.1239C=	NP_001159392.1:p.Arg413=
NM_001165921.1:c.1047C=	NP_001159393.1:p.Arg349=
XM_005256699.3:c.1344C=	XP_005256756.1:p.Arg448=
XM_005256700.3:c.1251C=	XP_005256757.1:p.Arg417=
XM_005256701.3:c.1287C=	XP_005256758.2:p.Arg429=
XM_005256703.3:c.1158C=	XP_005256760.1:p.Arg386=
XM_005256701.4:c.1287C=	XP_005256758.2:p.Arg429=
XM_017024765.1:c.1251C=	XP_016880254.1:p.Arg417=
XM_024450805.1:c.1251C=	XP_024306573.1:p.Arg417=
NM_000934.4:c.1239C= MANE Select	NP_000925.2:p.Arg413=
NM_001165921.2:c.1047C=	NP_001159393.1:p.Arg349=