Canonical Allele Identifier: CA353670962

Gene: PROS1

Linked Data

• dbSNP Id: rs1708200007
• MyVariant Identifiers: chr3:g.93595876T>C (hg19) ; chr3:g.93877032T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877032T>C , CM000665.2:g.93877032T>C	GRCh38
NC_000003.11:g.93595876T>C , CM000665.1:g.93595876T>C	GRCh37
NC_000003.10:g.95078566T>C	NCBI36
NG_009813.1:g.102059A>G , LRG_572:g.102059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1804A>G	ENSP00000330021.7:p.Arg602Gly
ENST00000394236.9:c.1804A>G MANE Select	ENSP00000377783.3:p.Arg602Gly
ENST00000407433.6:c.1759A>G	ENSP00000385794.2:p.Arg587Gly
ENST00000647936.1:c.1644+2131A>G	ENSP00000496822.1:n.1644+2131A>G
ENST00000648381.1:n.1972A>G
ENST00000648853.1:c.1762A>G	ENSP00000497262.1:p.Arg588Gly
ENST00000649585.1:c.747A>G	ENSP00000498163.1:n.747A>G
ENST00000650591.1:c.1900A>G	ENSP00000497376.1:p.Arg634Gly
ENST00000394236.7:c.1804A>G	ENSP00000377783.3:p.Arg602Gly
ENST00000407433.5:c.1411A>G	ENSP00000385794.1:p.Arg471Gly
NM_000313.3:c.1804A>G , LRG_572t1:c.1804A>G	NP_000304.2:p.Arg602Gly
NM_001314077.1:c.1900A>G , LRG_572t2:c.1900A>G	NP_001301006.1:p.Arg634Gly
NM_000313.4:c.1804A>G MANE Select	NP_000304.2:p.Arg602Gly
NM_001314077.2:c.1900A>G	NP_001301006.1:p.Arg634Gly