Canonical Allele Identifier: CA434464384

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598031C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879187C>T , CM000665.2:g.93879187C>T	GRCh38
NC_000003.11:g.93598031C>T , CM000665.1:g.93598031C>T	GRCh37
NC_000003.10:g.95080721C>T	NCBI36
NG_009813.1:g.99904G>A , LRG_572:g.99904G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1620G>A	ENSP00000330021.7:p.Val540=
ENST00000394236.9:c.1620G>A MANE Select	ENSP00000377783.3:p.Val540=
ENST00000407433.6:c.1575G>A	ENSP00000385794.2:p.Val525=
ENST00000647936.1:c.1620G>A	ENSP00000496822.1:p.Val540=
ENST00000648381.1:n.1788G>A
ENST00000648853.1:c.1578G>A	ENSP00000497262.1:p.Val526=
ENST00000649103.1:c.1719G>A	ENSP00000497962.1:n.1719G>A
ENST00000649585.1:c.563G>A	ENSP00000498163.1:n.563G>A
ENST00000650591.1:c.1716G>A	ENSP00000497376.1:p.Val572=
ENST00000394236.7:c.1620G>A	ENSP00000377783.3:p.Val540=
ENST00000407433.5:c.1227G>A	ENSP00000385794.1:p.Val409=
NM_000313.3:c.1620G>A , LRG_572t1:c.1620G>A	NP_000304.2:p.Val540=
NM_001314077.1:c.1716G>A , LRG_572t2:c.1716G>A	NP_001301006.1:p.Val572=
NM_000313.4:c.1620G>A MANE Select	NP_000304.2:p.Val540=
NM_001314077.2:c.1716G>A	NP_001301006.1:p.Val572=