Canonical Allele Identifier: CA353672069

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598108G>T (hg19) ; chr3:g.93879264G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879264G>T , CM000665.2:g.93879264G>T	GRCh38
NC_000003.11:g.93598108G>T , CM000665.1:g.93598108G>T	GRCh37
NC_000003.10:g.95080798G>T	NCBI36
NG_009813.1:g.99827C>A , LRG_572:g.99827C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1543C>A	ENSP00000330021.7:p.Arg515Ser
ENST00000394236.9:c.1543C>A MANE Select	ENSP00000377783.3:p.Arg515Ser
ENST00000407433.6:c.1498C>A	ENSP00000385794.2:p.Arg500Ser
ENST00000647936.1:c.1543C>A	ENSP00000496822.1:p.Arg515Ser
ENST00000648381.1:n.1711C>A
ENST00000648853.1:c.1501C>A	ENSP00000497262.1:p.Arg501Ser
ENST00000649103.1:c.1642C>A	ENSP00000497962.1:n.1642C>A
ENST00000649585.1:c.486C>A	ENSP00000498163.1:n.486C>A
ENST00000650591.1:c.1639C>A	ENSP00000497376.1:p.Arg547Ser
ENST00000394236.7:c.1543C>A	ENSP00000377783.3:p.Arg515Ser
ENST00000407433.5:c.1150C>A	ENSP00000385794.1:p.Arg384Ser
NM_000313.3:c.1543C>A , LRG_572t1:c.1543C>A	NP_000304.2:p.Arg515Ser
NM_001314077.1:c.1639C>A , LRG_572t2:c.1639C>A	NP_001301006.1:p.Arg547Ser
NM_000313.4:c.1543C>A MANE Select	NP_000304.2:p.Arg515Ser
NM_001314077.2:c.1639C>A	NP_001301006.1:p.Arg547Ser