Canonical Allele Identifier: CA2243019115

Gene: SERPINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754346G= , CM000679.2:g.1754346G=	GRCh38
NC_000017.10:g.1657640G= , CM000679.1:g.1657640G=	GRCh37
NC_000017.9:g.1604390G=	NCBI36
NG_013215.1:g.16511G= , LRG_885:g.16511G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1288G=	ENSP00000371493.4:p.Val430=
ENST00000453066.6:c.1288G= MANE Select	ENSP00000402286.2:p.Val430=
ENST00000324015.7:c.1288G=	ENSP00000321853.3:p.Val430=
ENST00000382061.4:c.1288G=	ENSP00000371493.4:p.Val430=
ENST00000450523.6:c.1096G=	ENSP00000403877.2:p.Val366=
NM_000934.3:c.1288G= , LRG_885t1:c.1288G=	NP_000925.2:p.Val430=
NM_001165920.1:c.1288G=	NP_001159392.1:p.Val430=
NM_001165921.1:c.1096G=	NP_001159393.1:p.Val366=
XM_005256699.3:c.1393G=	XP_005256756.1:p.Val465=
XM_005256700.3:c.1300G=	XP_005256757.1:p.Val434=
XM_005256701.3:c.1336G=	XP_005256758.2:p.Val446=
XM_005256703.3:c.1207G=	XP_005256760.1:p.Val403=
XM_005256701.4:c.1336G=	XP_005256758.2:p.Val446=
XM_017024765.1:c.1300G=	XP_016880254.1:p.Val434=
XM_024450805.1:c.1300G=	XP_024306573.1:p.Val434=
NM_000934.4:c.1288G= MANE Select	NP_000925.2:p.Val430=
NM_001165921.2:c.1096G=	NP_001159393.1:p.Val366=