Canonical Allele Identifier: CA1385026843
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874154T= , CM000665.2:g.93874154T= GRCh38
NC_000003.11:g.93592998T= , CM000665.1:g.93592998T= GRCh37
NC_000003.10:g.95075688T= NCBI36
NG_009813.1:g.104937A= , LRG_572:g.104937A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+90A= ENSP00000330021.7:n.*1+90A=
ENST00000394236.9:c.*91A= MANE Select ENSP00000377783.3:n.*91A=
ENST00000407433.6:c.*91A= ENSP00000385794.2:n.*91A=
ENST00000647936.1:c.*225A= ENSP00000496822.1:n.*225A=
ENST00000648381.1:n.2290A=
ENST00000648853.1:c.*91A= ENSP00000497262.1:n.*91A=
ENST00000650591.1:c.*91A= ENSP00000497376.1:n.*91A=
ENST00000394236.7:c.*91A= ENSP00000377783.3:n.*91A=
ENST00000407433.5:c.*91A= ENSP00000385794.1:n.*91A=
NM_000313.3:c.*91A= , LRG_572t1:c.*91A= NP_000304.2:n.*91A=
NM_001314077.1:c.*91A= , LRG_572t2:c.*91A= NP_001301006.1:n.*91A=
NM_000313.4:c.*91A= MANE Select NP_000304.2:n.*91A=
NM_001314077.2:c.*91A= NP_001301006.1:n.*91A=