Canonical Allele Identifier: CA397575609

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657635T>C (hg19) ; chr17:g.1754341T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754341T>C , CM000679.2:g.1754341T>C	GRCh38
NC_000017.10:g.1657635T>C , CM000679.1:g.1657635T>C	GRCh37
NC_000017.9:g.1604385T>C	NCBI36
NG_013215.1:g.16506T>C , LRG_885:g.16506T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1283T>C	ENSP00000371493.4:p.Leu428Pro
ENST00000453066.6:c.1283T>C MANE Select	ENSP00000402286.2:p.Leu428Pro
ENST00000324015.7:c.1283T>C	ENSP00000321853.3:p.Leu428Pro
ENST00000382061.4:c.1283T>C	ENSP00000371493.4:p.Leu428Pro
ENST00000450523.6:c.1091T>C	ENSP00000403877.2:p.Leu364Pro
NM_000934.3:c.1283T>C , LRG_885t1:c.1283T>C	NP_000925.2:p.Leu428Pro
NM_001165920.1:c.1283T>C	NP_001159392.1:p.Leu428Pro
NM_001165921.1:c.1091T>C	NP_001159393.1:p.Leu364Pro
XM_005256699.3:c.1388T>C	XP_005256756.1:p.Leu463Pro
XM_005256700.3:c.1295T>C	XP_005256757.1:p.Leu432Pro
XM_005256701.3:c.1331T>C	XP_005256758.2:p.Leu444Pro
XM_005256703.3:c.1202T>C	XP_005256760.1:p.Leu401Pro
XM_005256701.4:c.1331T>C	XP_005256758.2:p.Leu444Pro
XM_017024765.1:c.1295T>C	XP_016880254.1:p.Leu432Pro
XM_024450805.1:c.1295T>C	XP_024306573.1:p.Leu432Pro
NM_000934.4:c.1283T>C MANE Select	NP_000925.2:p.Leu428Pro
NM_001165921.2:c.1091T>C	NP_001159393.1:p.Leu364Pro