Canonical Allele Identifier: CA1385038307
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896609A= , CM000665.2:g.93896609A= GRCh38
NC_000003.11:g.93615453A= , CM000665.1:g.93615453A= GRCh37
NC_000003.10:g.95098143A= NCBI36
NG_009813.1:g.82482T= , LRG_572:g.82482T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.932T= ENSP00000330021.7:p.Leu311=
ENST00000394236.9:c.932T= MANE Select ENSP00000377783.3:p.Leu311=
ENST00000407433.6:c.887T= ENSP00000385794.2:p.Leu296=
ENST00000647936.1:c.932T= ENSP00000496822.1:p.Leu311=
ENST00000648381.1:n.1100T=
ENST00000648853.1:c.890T= ENSP00000497262.1:p.Leu297=
ENST00000649103.1:c.1031T= ENSP00000497962.1:n.1031T=
ENST00000650591.1:c.1028T= ENSP00000497376.1:p.Leu343=
ENST00000394236.7:c.932T= ENSP00000377783.3:p.Leu311=
ENST00000407433.5:c.539T= ENSP00000385794.1:p.Leu180=
NM_000313.3:c.932T= , LRG_572t1:c.932T= NP_000304.2:p.Leu311=
NM_001314077.1:c.1028T= , LRG_572t2:c.1028T= NP_001301006.1:p.Leu343=
NM_000313.4:c.932T= MANE Select NP_000304.2:p.Leu311=
NM_001314077.2:c.1028T= NP_001301006.1:p.Leu343=