Canonical Allele Identifier: CA497389608

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657633C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754339C>A , CM000679.2:g.1754339C>A	GRCh38
NC_000017.10:g.1657633C>A , CM000679.1:g.1657633C>A	GRCh37
NC_000017.9:g.1604383C>A	NCBI36
NG_013215.1:g.16504C>A , LRG_885:g.16504C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1281C>A	ENSP00000371493.4:p.Pro427=
ENST00000453066.6:c.1281C>A MANE Select	ENSP00000402286.2:p.Pro427=
ENST00000324015.7:c.1281C>A	ENSP00000321853.3:p.Pro427=
ENST00000382061.4:c.1281C>A	ENSP00000371493.4:p.Pro427=
ENST00000450523.6:c.1089C>A	ENSP00000403877.2:p.Pro363=
NM_000934.3:c.1281C>A , LRG_885t1:c.1281C>A	NP_000925.2:p.Pro427=
NM_001165920.1:c.1281C>A	NP_001159392.1:p.Pro427=
NM_001165921.1:c.1089C>A	NP_001159393.1:p.Pro363=
XM_005256699.3:c.1386C>A	XP_005256756.1:p.Pro462=
XM_005256700.3:c.1293C>A	XP_005256757.1:p.Pro431=
XM_005256701.3:c.1329C>A	XP_005256758.2:p.Pro443=
XM_005256703.3:c.1200C>A	XP_005256760.1:p.Pro400=
XM_005256701.4:c.1329C>A	XP_005256758.2:p.Pro443=
XM_017024765.1:c.1293C>A	XP_016880254.1:p.Pro431=
XM_024450805.1:c.1293C>A	XP_024306573.1:p.Pro431=
NM_000934.4:c.1281C>A MANE Select	NP_000925.2:p.Pro427=
NM_001165921.2:c.1089C>A	NP_001159393.1:p.Pro363=