Canonical Allele Identifier: CA353672918

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93617357C>T (hg19) ; chr3:g.93898513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898513C>T , CM000665.2:g.93898513C>T	GRCh38
NC_000003.11:g.93617357C>T , CM000665.1:g.93617357C>T	GRCh37
NC_000003.10:g.95100047C>T	NCBI36
NG_009813.1:g.80578G>A , LRG_572:g.80578G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.784G>A	ENSP00000330021.7:p.Gly262Ser
ENST00000394236.9:c.784G>A MANE Select	ENSP00000377783.3:p.Gly262Ser
ENST00000407433.6:c.739G>A	ENSP00000385794.2:p.Gly247Ser
ENST00000647936.1:c.784G>A	ENSP00000496822.1:p.Gly262Ser
ENST00000648381.1:n.952G>A
ENST00000648853.1:c.742G>A	ENSP00000497262.1:p.Gly248Ser
ENST00000649103.1:c.883G>A	ENSP00000497962.1:n.883G>A
ENST00000650591.1:c.880G>A	ENSP00000497376.1:p.Gly294Ser
ENST00000394236.7:c.784G>A	ENSP00000377783.3:p.Gly262Ser
ENST00000407433.5:c.391G>A	ENSP00000385794.1:p.Gly131Ser
NM_000313.3:c.784G>A , LRG_572t1:c.784G>A	NP_000304.2:p.Gly262Ser
NM_001314077.1:c.880G>A , LRG_572t2:c.880G>A	NP_001301006.1:p.Gly294Ser
NM_000313.4:c.784G>A MANE Select	NP_000304.2:p.Gly262Ser
NM_001314077.2:c.880G>A	NP_001301006.1:p.Gly294Ser