Canonical Allele Identifier: CA434462782

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593113A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874269A>T , CM000665.2:g.93874269A>T	GRCh38
NC_000003.11:g.93593113A>T , CM000665.1:g.93593113A>T	GRCh37
NC_000003.10:g.95075803A>T	NCBI36
NG_009813.1:g.104822T>A , LRG_572:g.104822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.2007T>A	ENSP00000330021.7:p.Val669=
ENST00000394236.9:c.2007T>A MANE Select	ENSP00000377783.3:p.Val669=
ENST00000407433.6:c.1962T>A	ENSP00000385794.2:p.Val654=
ENST00000647936.1:c.*110T>A	ENSP00000496822.1:n.*110T>A
ENST00000648381.1:n.2175T>A
ENST00000648853.1:c.1965T>A	ENSP00000497262.1:p.Val655=
ENST00000650591.1:c.2103T>A	ENSP00000497376.1:p.Val701=
ENST00000394236.7:c.2007T>A	ENSP00000377783.3:p.Val669=
ENST00000407433.5:c.1614T>A	ENSP00000385794.1:p.Val538=
NM_000313.3:c.2007T>A , LRG_572t1:c.2007T>A	NP_000304.2:p.Val669=
NM_001314077.1:c.2103T>A , LRG_572t2:c.2103T>A	NP_001301006.1:p.Val701=
NM_000313.4:c.2007T>A MANE Select	NP_000304.2:p.Val669=
NM_001314077.2:c.2103T>A	NP_001301006.1:p.Val701=