Canonical Allele Identifier: CA434462829

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593155A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874311A>T , CM000665.2:g.93874311A>T	GRCh38
NC_000003.11:g.93593155A>T , CM000665.1:g.93593155A>T	GRCh37
NC_000003.10:g.95075845A>T	NCBI36
NG_009813.1:g.104780T>A , LRG_572:g.104780T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1965T>A	ENSP00000330021.7:p.Ile655=
ENST00000394236.9:c.1965T>A MANE Select	ENSP00000377783.3:p.Ile655=
ENST00000407433.6:c.1920T>A	ENSP00000385794.2:p.Ile640=
ENST00000647936.1:c.*68T>A	ENSP00000496822.1:n.*68T>A
ENST00000648381.1:n.2133T>A
ENST00000648853.1:c.1923T>A	ENSP00000497262.1:p.Ile641=
ENST00000650591.1:c.2061T>A	ENSP00000497376.1:p.Ile687=
ENST00000394236.7:c.1965T>A	ENSP00000377783.3:p.Ile655=
ENST00000407433.5:c.1572T>A	ENSP00000385794.1:p.Ile524=
NM_000313.3:c.1965T>A , LRG_572t1:c.1965T>A	NP_000304.2:p.Ile655=
NM_001314077.1:c.2061T>A , LRG_572t2:c.2061T>A	NP_001301006.1:p.Ile687=
NM_000313.4:c.1965T>A MANE Select	NP_000304.2:p.Ile655=
NM_001314077.2:c.2061T>A	NP_001301006.1:p.Ile687=