Canonical Allele Identifier: CA353672522

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615429T>A (hg19) ; chr3:g.93896585T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896585T>A , CM000665.2:g.93896585T>A	GRCh38
NC_000003.11:g.93615429T>A , CM000665.1:g.93615429T>A	GRCh37
NC_000003.10:g.95098119T>A	NCBI36
NG_009813.1:g.82506A>T , LRG_572:g.82506A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.956A>T	ENSP00000330021.7:p.Glu319Val
ENST00000394236.9:c.956A>T MANE Select	ENSP00000377783.3:p.Glu319Val
ENST00000407433.6:c.911A>T	ENSP00000385794.2:p.Glu304Val
ENST00000647936.1:c.956A>T	ENSP00000496822.1:p.Glu319Val
ENST00000648381.1:n.1124A>T
ENST00000648853.1:c.914A>T	ENSP00000497262.1:p.Glu305Val
ENST00000649103.1:c.1055A>T	ENSP00000497962.1:n.1055A>T
ENST00000650591.1:c.1052A>T	ENSP00000497376.1:p.Glu351Val
ENST00000394236.7:c.956A>T	ENSP00000377783.3:p.Glu319Val
ENST00000407433.5:c.563A>T	ENSP00000385794.1:p.Glu188Val
NM_000313.3:c.956A>T , LRG_572t1:c.956A>T	NP_000304.2:p.Glu319Val
NM_001314077.1:c.1052A>T , LRG_572t2:c.1052A>T	NP_001301006.1:p.Glu351Val
NM_000313.4:c.956A>T MANE Select	NP_000304.2:p.Glu319Val
NM_001314077.2:c.1052A>T	NP_001301006.1:p.Glu351Val