Canonical Allele Identifier: CA397575621

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657638T>C (hg19) ; chr17:g.1754344T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754344T>C , CM000679.2:g.1754344T>C	GRCh38
NC_000017.10:g.1657638T>C , CM000679.1:g.1657638T>C	GRCh37
NC_000017.9:g.1604388T>C	NCBI36
NG_013215.1:g.16509T>C , LRG_885:g.16509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1286T>C	ENSP00000371493.4:p.Phe429Ser
ENST00000453066.6:c.1286T>C MANE Select	ENSP00000402286.2:p.Phe429Ser
ENST00000324015.7:c.1286T>C	ENSP00000321853.3:p.Phe429Ser
ENST00000382061.4:c.1286T>C	ENSP00000371493.4:p.Phe429Ser
ENST00000450523.6:c.1094T>C	ENSP00000403877.2:p.Phe365Ser
NM_000934.3:c.1286T>C , LRG_885t1:c.1286T>C	NP_000925.2:p.Phe429Ser
NM_001165920.1:c.1286T>C	NP_001159392.1:p.Phe429Ser
NM_001165921.1:c.1094T>C	NP_001159393.1:p.Phe365Ser
XM_005256699.3:c.1391T>C	XP_005256756.1:p.Phe464Ser
XM_005256700.3:c.1298T>C	XP_005256757.1:p.Phe433Ser
XM_005256701.3:c.1334T>C	XP_005256758.2:p.Phe445Ser
XM_005256703.3:c.1205T>C	XP_005256760.1:p.Phe402Ser
XM_005256701.4:c.1334T>C	XP_005256758.2:p.Phe445Ser
XM_017024765.1:c.1298T>C	XP_016880254.1:p.Phe433Ser
XM_024450805.1:c.1298T>C	XP_024306573.1:p.Phe433Ser
NM_000934.4:c.1286T>C MANE Select	NP_000925.2:p.Phe429Ser
NM_001165921.2:c.1094T>C	NP_001159393.1:p.Phe365Ser