Canonical Allele Identifier: CA434464474

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598136A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879292A>T , CM000665.2:g.93879292A>T	GRCh38
NC_000003.11:g.93598136A>T , CM000665.1:g.93598136A>T	GRCh37
NC_000003.10:g.95080826A>T	NCBI36
NG_009813.1:g.99799T>A , LRG_572:g.99799T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1515T>A	ENSP00000330021.7:p.Gly505=
ENST00000394236.9:c.1515T>A MANE Select	ENSP00000377783.3:p.Gly505=
ENST00000407433.6:c.1470T>A	ENSP00000385794.2:p.Gly490=
ENST00000647936.1:c.1515T>A	ENSP00000496822.1:p.Gly505=
ENST00000648381.1:n.1683T>A
ENST00000648853.1:c.1473T>A	ENSP00000497262.1:p.Gly491=
ENST00000649103.1:c.1614T>A	ENSP00000497962.1:n.1614T>A
ENST00000649585.1:c.458T>A	ENSP00000498163.1:n.458T>A
ENST00000650591.1:c.1611T>A	ENSP00000497376.1:p.Gly537=
ENST00000394236.7:c.1515T>A	ENSP00000377783.3:p.Gly505=
ENST00000407433.5:c.1122T>A	ENSP00000385794.1:p.Gly374=
NM_000313.3:c.1515T>A , LRG_572t1:c.1515T>A	NP_000304.2:p.Gly505=
NM_001314077.1:c.1611T>A , LRG_572t2:c.1611T>A	NP_001301006.1:p.Gly537=
NM_000313.4:c.1515T>A MANE Select	NP_000304.2:p.Gly505=
NM_001314077.2:c.1611T>A	NP_001301006.1:p.Gly537=