Canonical Allele Identifier: CA397575460

Gene: SERPINF2

Linked Data

• dbSNP Id: rs1310159441
• gnomAD v4: 17-1754321-G-C
• MyVariant Identifiers: chr17:g.1657615G>C (hg19) ; chr17:g.1754321G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754321G>C , CM000679.2:g.1754321G>C	GRCh38
NC_000017.10:g.1657615G>C , CM000679.1:g.1657615G>C	GRCh37
NC_000017.9:g.1604365G>C	NCBI36
NG_013215.1:g.16486G>C , LRG_885:g.16486G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1263G>C	ENSP00000371493.4:p.Glu421Asp
ENST00000453066.6:c.1263G>C MANE Select	ENSP00000402286.2:p.Glu421Asp
ENST00000324015.7:c.1263G>C	ENSP00000321853.3:p.Glu421Asp
ENST00000382061.4:c.1263G>C	ENSP00000371493.4:p.Glu421Asp
ENST00000450523.6:c.1071G>C	ENSP00000403877.2:p.Glu357Asp
NM_000934.3:c.1263G>C , LRG_885t1:c.1263G>C	NP_000925.2:p.Glu421Asp
NM_001165920.1:c.1263G>C	NP_001159392.1:p.Glu421Asp
NM_001165921.1:c.1071G>C	NP_001159393.1:p.Glu357Asp
XM_005256699.3:c.1368G>C	XP_005256756.1:p.Glu456Asp
XM_005256700.3:c.1275G>C	XP_005256757.1:p.Glu425Asp
XM_005256701.3:c.1311G>C	XP_005256758.2:p.Glu437Asp
XM_005256703.3:c.1182G>C	XP_005256760.1:p.Glu394Asp
XM_005256701.4:c.1311G>C	XP_005256758.2:p.Glu437Asp
XM_017024765.1:c.1275G>C	XP_016880254.1:p.Glu425Asp
XM_024450805.1:c.1275G>C	XP_024306573.1:p.Glu425Asp
NM_000934.4:c.1263G>C MANE Select	NP_000925.2:p.Glu421Asp
NM_001165921.2:c.1071G>C	NP_001159393.1:p.Glu357Asp