Canonical Allele Identifier: CA353672899

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93617348A>T (hg19) ; chr3:g.93898504A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898504A>T , CM000665.2:g.93898504A>T	GRCh38
NC_000003.11:g.93617348A>T , CM000665.1:g.93617348A>T	GRCh37
NC_000003.10:g.95100038A>T	NCBI36
NG_009813.1:g.80587T>A , LRG_572:g.80587T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.793T>A	ENSP00000330021.7:p.Cys265Ser
ENST00000394236.9:c.793T>A MANE Select	ENSP00000377783.3:p.Cys265Ser
ENST00000407433.6:c.748T>A	ENSP00000385794.2:p.Cys250Ser
ENST00000647936.1:c.793T>A	ENSP00000496822.1:p.Cys265Ser
ENST00000648381.1:n.961T>A
ENST00000648853.1:c.751T>A	ENSP00000497262.1:p.Cys251Ser
ENST00000649103.1:c.892T>A	ENSP00000497962.1:n.892T>A
ENST00000650591.1:c.889T>A	ENSP00000497376.1:p.Cys297Ser
ENST00000394236.7:c.793T>A	ENSP00000377783.3:p.Cys265Ser
ENST00000407433.5:c.400T>A	ENSP00000385794.1:p.Cys134Ser
NM_000313.3:c.793T>A , LRG_572t1:c.793T>A	NP_000304.2:p.Cys265Ser
NM_001314077.1:c.889T>A , LRG_572t2:c.889T>A	NP_001301006.1:p.Cys297Ser
NM_000313.4:c.793T>A MANE Select	NP_000304.2:p.Cys265Ser
NM_001314077.2:c.889T>A	NP_001301006.1:p.Cys297Ser