Canonical Allele Identifier: CA2503334
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs776171385
gnomAD v2: 3-93615498-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896654T>A , CM000665.2:g.93896654T>A GRCh38
NC_000003.11:g.93615498T>A , CM000665.1:g.93615498T>A GRCh37
NC_000003.10:g.95098188T>A NCBI36
NG_009813.1:g.82437A>T , LRG_572:g.82437A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.887A>T ENSP00000330021.7:p.Lys296Met
ENST00000394236.9:c.887A>T MANE Select ENSP00000377783.3:p.Lys296Met
ENST00000407433.6:c.842A>T ENSP00000385794.2:p.Lys281Met
ENST00000647936.1:c.887A>T ENSP00000496822.1:p.Lys296Met
ENST00000648381.1:n.1055A>T
ENST00000648853.1:c.845A>T ENSP00000497262.1:p.Lys282Met
ENST00000649103.1:c.986A>T ENSP00000497962.1:n.986A>T
ENST00000650591.1:c.983A>T ENSP00000497376.1:p.Lys328Met
ENST00000394236.7:c.887A>T ENSP00000377783.3:p.Lys296Met
ENST00000407433.5:c.494A>T ENSP00000385794.1:p.Lys165Met
NM_000313.3:c.887A>T , LRG_572t1:c.887A>T NP_000304.2:p.Lys296Met
NM_001314077.1:c.983A>T , LRG_572t2:c.983A>T NP_001301006.1:p.Lys328Met
NM_000313.4:c.887A>T MANE Select NP_000304.2:p.Lys296Met
NM_001314077.2:c.983A>T NP_001301006.1:p.Lys328Met