Canonical Allele Identifier: CA353672625

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615477G>C (hg19) ; chr3:g.93896633G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896633G>C , CM000665.2:g.93896633G>C	GRCh38
NC_000003.11:g.93615477G>C , CM000665.1:g.93615477G>C	GRCh37
NC_000003.10:g.95098167G>C	NCBI36
NG_009813.1:g.82458C>G , LRG_572:g.82458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.908C>G	ENSP00000330021.7:p.Ala303Gly
ENST00000394236.9:c.908C>G MANE Select	ENSP00000377783.3:p.Ala303Gly
ENST00000407433.6:c.863C>G	ENSP00000385794.2:p.Ala288Gly
ENST00000647936.1:c.908C>G	ENSP00000496822.1:p.Ala303Gly
ENST00000648381.1:n.1076C>G
ENST00000648853.1:c.866C>G	ENSP00000497262.1:p.Ala289Gly
ENST00000649103.1:c.1007C>G	ENSP00000497962.1:n.1007C>G
ENST00000650591.1:c.1004C>G	ENSP00000497376.1:p.Ala335Gly
ENST00000394236.7:c.908C>G	ENSP00000377783.3:p.Ala303Gly
ENST00000407433.5:c.515C>G	ENSP00000385794.1:p.Ala172Gly
NM_000313.3:c.908C>G , LRG_572t1:c.908C>G	NP_000304.2:p.Ala303Gly
NM_001314077.1:c.1004C>G , LRG_572t2:c.1004C>G	NP_001301006.1:p.Ala335Gly
NM_000313.4:c.908C>G MANE Select	NP_000304.2:p.Ala303Gly
NM_001314077.2:c.1004C>G	NP_001301006.1:p.Ala335Gly