Canonical Allele Identifier: CA397575750

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657662A>T (hg19) ; chr17:g.1754368A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754368A>T , CM000679.2:g.1754368A>T	GRCh38
NC_000017.10:g.1657662A>T , CM000679.1:g.1657662A>T	GRCh37
NC_000017.9:g.1604412A>T	NCBI36
NG_013215.1:g.16533A>T , LRG_885:g.16533A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1310A>T	ENSP00000371493.4:p.Asn437Ile
ENST00000453066.6:c.1310A>T MANE Select	ENSP00000402286.2:p.Asn437Ile
ENST00000324015.7:c.1310A>T	ENSP00000321853.3:p.Asn437Ile
ENST00000382061.4:c.1310A>T	ENSP00000371493.4:p.Asn437Ile
ENST00000450523.6:c.1118A>T	ENSP00000403877.2:p.Asn373Ile
NM_000934.3:c.1310A>T , LRG_885t1:c.1310A>T	NP_000925.2:p.Asn437Ile
NM_001165920.1:c.1310A>T	NP_001159392.1:p.Asn437Ile
NM_001165921.1:c.1118A>T	NP_001159393.1:p.Asn373Ile
XM_005256699.3:c.1415A>T	XP_005256756.1:p.Asn472Ile
XM_005256700.3:c.1322A>T	XP_005256757.1:p.Asn441Ile
XM_005256701.3:c.1358A>T	XP_005256758.2:p.Asn453Ile
XM_005256703.3:c.1229A>T	XP_005256760.1:p.Asn410Ile
XM_005256701.4:c.1358A>T	XP_005256758.2:p.Asn453Ile
XM_017024765.1:c.1322A>T	XP_016880254.1:p.Asn441Ile
XM_024450805.1:c.1322A>T	XP_024306573.1:p.Asn441Ile
NM_000934.4:c.1310A>T MANE Select	NP_000925.2:p.Asn437Ile
NM_001165921.2:c.1118A>T	NP_001159393.1:p.Asn373Ile