Canonical Allele Identifier: CA353672138

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598129C>T (hg19) ; chr3:g.93879285C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879285C>T , CM000665.2:g.93879285C>T	GRCh38
NC_000003.11:g.93598129C>T , CM000665.1:g.93598129C>T	GRCh37
NC_000003.10:g.95080819C>T	NCBI36
NG_009813.1:g.99806G>A , LRG_572:g.99806G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1522G>A	ENSP00000330021.7:p.Val508Ile
ENST00000394236.9:c.1522G>A MANE Select	ENSP00000377783.3:p.Val508Ile
ENST00000407433.6:c.1477G>A	ENSP00000385794.2:p.Val493Ile
ENST00000647936.1:c.1522G>A	ENSP00000496822.1:p.Val508Ile
ENST00000648381.1:n.1690G>A
ENST00000648853.1:c.1480G>A	ENSP00000497262.1:p.Val494Ile
ENST00000649103.1:c.1621G>A	ENSP00000497962.1:n.1621G>A
ENST00000649585.1:c.465G>A	ENSP00000498163.1:n.465G>A
ENST00000650591.1:c.1618G>A	ENSP00000497376.1:p.Val540Ile
ENST00000394236.7:c.1522G>A	ENSP00000377783.3:p.Val508Ile
ENST00000407433.5:c.1129G>A	ENSP00000385794.1:p.Val377Ile
NM_000313.3:c.1522G>A , LRG_572t1:c.1522G>A	NP_000304.2:p.Val508Ile
NM_001314077.1:c.1618G>A , LRG_572t2:c.1618G>A	NP_001301006.1:p.Val540Ile
NM_000313.4:c.1522G>A MANE Select	NP_000304.2:p.Val508Ile
NM_001314077.2:c.1618G>A	NP_001301006.1:p.Val540Ile