Canonical Allele Identifier: CA353672734

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615525A>T (hg19) ; chr3:g.93896681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896681A>T , CM000665.2:g.93896681A>T	GRCh38
NC_000003.11:g.93615525A>T , CM000665.1:g.93615525A>T	GRCh37
NC_000003.10:g.95098215A>T	NCBI36
NG_009813.1:g.82410T>A , LRG_572:g.82410T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.860T>A	ENSP00000330021.7:p.Val287Glu
ENST00000394236.9:c.860T>A MANE Select	ENSP00000377783.3:p.Val287Glu
ENST00000407433.6:c.815T>A	ENSP00000385794.2:p.Val272Glu
ENST00000647936.1:c.860T>A	ENSP00000496822.1:p.Val287Glu
ENST00000648381.1:n.1028T>A
ENST00000648853.1:c.818T>A	ENSP00000497262.1:p.Val273Glu
ENST00000649103.1:c.959T>A	ENSP00000497962.1:n.959T>A
ENST00000650591.1:c.956T>A	ENSP00000497376.1:p.Val319Glu
ENST00000394236.7:c.860T>A	ENSP00000377783.3:p.Val287Glu
ENST00000407433.5:c.467T>A	ENSP00000385794.1:p.Val156Glu
NM_000313.3:c.860T>A , LRG_572t1:c.860T>A	NP_000304.2:p.Val287Glu
NM_001314077.1:c.956T>A , LRG_572t2:c.956T>A	NP_001301006.1:p.Val319Glu
NM_000313.4:c.860T>A MANE Select	NP_000304.2:p.Val287Glu
NM_001314077.2:c.956T>A	NP_001301006.1:p.Val319Glu