Canonical Allele Identifier: CA353670900

Gene: PROS1

Linked Data

• dbSNP Id: rs1708199402
• MyVariant Identifiers: chr3:g.93595852C>T (hg19) ; chr3:g.93877008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877008C>T , CM000665.2:g.93877008C>T	GRCh38
NC_000003.11:g.93595852C>T , CM000665.1:g.93595852C>T	GRCh37
NC_000003.10:g.95078542C>T	NCBI36
NG_009813.1:g.102083G>A , LRG_572:g.102083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1828G>A	ENSP00000330021.7:p.Ala610Thr
ENST00000394236.9:c.1828G>A MANE Select	ENSP00000377783.3:p.Ala610Thr
ENST00000407433.6:c.1783G>A	ENSP00000385794.2:p.Ala595Thr
ENST00000647936.1:c.1644+2155G>A	ENSP00000496822.1:n.1644+2155G>A
ENST00000648381.1:n.1996G>A
ENST00000648853.1:c.1786G>A	ENSP00000497262.1:p.Ala596Thr
ENST00000649585.1:c.771G>A	ENSP00000498163.1:n.771G>A
ENST00000650591.1:c.1924G>A	ENSP00000497376.1:p.Ala642Thr
ENST00000394236.7:c.1828G>A	ENSP00000377783.3:p.Ala610Thr
ENST00000407433.5:c.1435G>A	ENSP00000385794.1:p.Ala479Thr
NM_000313.3:c.1828G>A , LRG_572t1:c.1828G>A	NP_000304.2:p.Ala610Thr
NM_001314077.1:c.1924G>A , LRG_572t2:c.1924G>A	NP_001301006.1:p.Ala642Thr
NM_000313.4:c.1828G>A MANE Select	NP_000304.2:p.Ala610Thr
NM_001314077.2:c.1924G>A	NP_001301006.1:p.Ala642Thr