Canonical Allele Identifier: CA397575590

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657631C>A (hg19) ; chr17:g.1754337C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754337C>A , CM000679.2:g.1754337C>A	GRCh38
NC_000017.10:g.1657631C>A , CM000679.1:g.1657631C>A	GRCh37
NC_000017.9:g.1604381C>A	NCBI36
NG_013215.1:g.16502C>A , LRG_885:g.16502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1279C>A	ENSP00000371493.4:p.Pro427Thr
ENST00000453066.6:c.1279C>A MANE Select	ENSP00000402286.2:p.Pro427Thr
ENST00000324015.7:c.1279C>A	ENSP00000321853.3:p.Pro427Thr
ENST00000382061.4:c.1279C>A	ENSP00000371493.4:p.Pro427Thr
ENST00000450523.6:c.1087C>A	ENSP00000403877.2:p.Pro363Thr
NM_000934.3:c.1279C>A , LRG_885t1:c.1279C>A	NP_000925.2:p.Pro427Thr
NM_001165920.1:c.1279C>A	NP_001159392.1:p.Pro427Thr
NM_001165921.1:c.1087C>A	NP_001159393.1:p.Pro363Thr
XM_005256699.3:c.1384C>A	XP_005256756.1:p.Pro462Thr
XM_005256700.3:c.1291C>A	XP_005256757.1:p.Pro431Thr
XM_005256701.3:c.1327C>A	XP_005256758.2:p.Pro443Thr
XM_005256703.3:c.1198C>A	XP_005256760.1:p.Pro400Thr
XM_005256701.4:c.1327C>A	XP_005256758.2:p.Pro443Thr
XM_017024765.1:c.1291C>A	XP_016880254.1:p.Pro431Thr
XM_024450805.1:c.1291C>A	XP_024306573.1:p.Pro431Thr
NM_000934.4:c.1279C>A MANE Select	NP_000925.2:p.Pro427Thr
NM_001165921.2:c.1087C>A	NP_001159393.1:p.Pro363Thr