Canonical Allele Identifier: CA434464469

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598127T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879283T>A , CM000665.2:g.93879283T>A	GRCh38
NC_000003.11:g.93598127T>A , CM000665.1:g.93598127T>A	GRCh37
NC_000003.10:g.95080817T>A	NCBI36
NG_009813.1:g.99808A>T , LRG_572:g.99808A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1524A>T	ENSP00000330021.7:p.Val508=
ENST00000394236.9:c.1524A>T MANE Select	ENSP00000377783.3:p.Val508=
ENST00000407433.6:c.1479A>T	ENSP00000385794.2:p.Val493=
ENST00000647936.1:c.1524A>T	ENSP00000496822.1:p.Val508=
ENST00000648381.1:n.1692A>T
ENST00000648853.1:c.1482A>T	ENSP00000497262.1:p.Val494=
ENST00000649103.1:c.1623A>T	ENSP00000497962.1:n.1623A>T
ENST00000649585.1:c.467A>T	ENSP00000498163.1:n.467A>T
ENST00000650591.1:c.1620A>T	ENSP00000497376.1:p.Val540=
ENST00000394236.7:c.1524A>T	ENSP00000377783.3:p.Val508=
ENST00000407433.5:c.1131A>T	ENSP00000385794.1:p.Val377=
NM_000313.3:c.1524A>T , LRG_572t1:c.1524A>T	NP_000304.2:p.Val508=
NM_001314077.1:c.1620A>T , LRG_572t2:c.1620A>T	NP_001301006.1:p.Val540=
NM_000313.4:c.1524A>T MANE Select	NP_000304.2:p.Val508=
NM_001314077.2:c.1620A>T	NP_001301006.1:p.Val540=