Canonical Allele Identifier: CA1385026895
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874245T= , CM000665.2:g.93874245T= GRCh38
NC_000003.11:g.93593089T= , CM000665.1:g.93593089T= GRCh37
NC_000003.10:g.95075779T= NCBI36
NG_009813.1:g.104846A= , LRG_572:g.104846A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.2031A= ENSP00000330021.7:p.Ter677=
ENST00000394236.9:c.2031A= MANE Select ENSP00000377783.3:p.Ter677=
ENST00000407433.6:c.1986A= ENSP00000385794.2:p.Ter662=
ENST00000647936.1:c.*134A= ENSP00000496822.1:n.*134A=
ENST00000648381.1:n.2199A=
ENST00000648853.1:c.1989A= ENSP00000497262.1:p.Ter663=
ENST00000650591.1:c.2127A= ENSP00000497376.1:p.Ter709=
ENST00000394236.7:c.2031A= ENSP00000377783.3:p.Ter677=
ENST00000407433.5:c.1638A= ENSP00000385794.1:p.Ter546=
NM_000313.3:c.2031A= , LRG_572t1:c.2031A= NP_000304.2:p.Ter677=
NM_001314077.1:c.2127A= , LRG_572t2:c.2127A= NP_001301006.1:p.Ter709=
NM_000313.4:c.2031A= MANE Select NP_000304.2:p.Ter677=
NM_001314077.2:c.2127A= NP_001301006.1:p.Ter709=