Canonical Allele Identifier: CA915940533
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93898516del , CM000665.2:g.93898516del GRCh38
NC_000003.11:g.93617360del , CM000665.1:g.93617360del GRCh37
NC_000003.10:g.95100050del NCBI36
NG_009813.1:g.80576del , LRG_572:g.80576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.782del ENSP00000330021.7:p.Gly261GlufsTer?
ENST00000394236.9:c.782del MANE Select ENSP00000377783.3:p.Gly261GlufsTer?
ENST00000407433.6:c.737del ENSP00000385794.2:p.Gly246GlufsTer?
ENST00000647936.1:c.782del ENSP00000496822.1:p.Gly261GlufsTer?
ENST00000648381.1:n.950del
ENST00000648853.1:c.740del ENSP00000497262.1:p.Gly247GlufsTer?
ENST00000649103.1:c.881del ENSP00000497962.1:n.881del
ENST00000650591.1:c.878del ENSP00000497376.1:p.Gly293GlufsTer?
ENST00000394236.7:c.782del ENSP00000377783.3:p.Gly261GlufsTer?
ENST00000407433.5:c.389del ENSP00000385794.1:p.Gly130GlufsTer?
NM_000313.3:c.782del , LRG_572t1:c.782del NP_000304.2:p.Gly261GlufsTer?
NM_001314077.1:c.878del , LRG_572t2:c.878del NP_001301006.1:p.Gly293GlufsTer?
NM_000313.4:c.782del MANE Select NP_000304.2:p.Gly261GlufsTer?
NM_001314077.2:c.878del NP_001301006.1:p.Gly293GlufsTer?