Canonical Allele Identifier: CA497389639

Gene: SERPINF2

Linked Data

• MyVariant Identifiers: chr17:g.1657660C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1754366C>G , CM000679.2:g.1754366C>G	GRCh38
NC_000017.10:g.1657660C>G , CM000679.1:g.1657660C>G	GRCh37
NC_000017.9:g.1604410C>G	NCBI36
NG_013215.1:g.16531C>G , LRG_885:g.16531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382061.5:c.1308C>G	ENSP00000371493.4:p.Pro436=
ENST00000453066.6:c.1308C>G MANE Select	ENSP00000402286.2:p.Pro436=
ENST00000324015.7:c.1308C>G	ENSP00000321853.3:p.Pro436=
ENST00000382061.4:c.1308C>G	ENSP00000371493.4:p.Pro436=
ENST00000450523.6:c.1116C>G	ENSP00000403877.2:p.Pro372=
NM_000934.3:c.1308C>G , LRG_885t1:c.1308C>G	NP_000925.2:p.Pro436=
NM_001165920.1:c.1308C>G	NP_001159392.1:p.Pro436=
NM_001165921.1:c.1116C>G	NP_001159393.1:p.Pro372=
XM_005256699.3:c.1413C>G	XP_005256756.1:p.Pro471=
XM_005256700.3:c.1320C>G	XP_005256757.1:p.Pro440=
XM_005256701.3:c.1356C>G	XP_005256758.2:p.Pro452=
XM_005256703.3:c.1227C>G	XP_005256760.1:p.Pro409=
XM_005256701.4:c.1356C>G	XP_005256758.2:p.Pro452=
XM_017024765.1:c.1320C>G	XP_016880254.1:p.Pro440=
XM_024450805.1:c.1320C>G	XP_024306573.1:p.Pro440=
NM_000934.4:c.1308C>G MANE Select	NP_000925.2:p.Pro436=
NM_001165921.2:c.1116C>G	NP_001159393.1:p.Pro372=