Canonical Allele Identifier: CA8274430

Gene: SERPINF2

Linked Data

• dbSNP Id: rs149997779
• ExAC: 17:1657646 A / G
• gnomAD v4: 17-1754352-A-G
• MyVariant Identifiers: chr17:g.1657646A>G (hg19) ; chr17:g.1754352A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754352A>G , CM000679.2:g.1754352A>G	GRCh38
NC_000017.10:g.1657646A>G , CM000679.1:g.1657646A>G	GRCh37
NC_000017.9:g.1604396A>G	NCBI36
NG_013215.1:g.16517A>G , LRG_885:g.16517A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1294A>G	ENSP00000371493.4:p.Ser432Gly
ENST00000453066.6:c.1294A>G MANE Select	ENSP00000402286.2:p.Ser432Gly
ENST00000324015.7:c.1294A>G	ENSP00000321853.3:p.Ser432Gly
ENST00000382061.4:c.1294A>G	ENSP00000371493.4:p.Ser432Gly
ENST00000450523.6:c.1102A>G	ENSP00000403877.2:p.Ser368Gly
NM_000934.3:c.1294A>G , LRG_885t1:c.1294A>G	NP_000925.2:p.Ser432Gly
NM_001165920.1:c.1294A>G	NP_001159392.1:p.Ser432Gly
NM_001165921.1:c.1102A>G	NP_001159393.1:p.Ser368Gly
XM_005256699.3:c.1399A>G	XP_005256756.1:p.Ser467Gly
XM_005256700.3:c.1306A>G	XP_005256757.1:p.Ser436Gly
XM_005256701.3:c.1342A>G	XP_005256758.2:p.Ser448Gly
XM_005256703.3:c.1213A>G	XP_005256760.1:p.Ser405Gly
XM_005256701.4:c.1342A>G	XP_005256758.2:p.Ser448Gly
XM_017024765.1:c.1306A>G	XP_016880254.1:p.Ser436Gly
XM_024450805.1:c.1306A>G	XP_024306573.1:p.Ser436Gly
NM_000934.4:c.1294A>G MANE Select	NP_000925.2:p.Ser432Gly
NM_001165921.2:c.1102A>G	NP_001159393.1:p.Ser368Gly