Canonical Allele Identifier: CA1385026841
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874147C= , CM000665.2:g.93874147C= GRCh38
NC_000003.11:g.93592991C= , CM000665.1:g.93592991C= GRCh37
NC_000003.10:g.95075681C= NCBI36
NG_009813.1:g.104944G= , LRG_572:g.104944G=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+97G= ENSP00000330021.7:n.*1+97G=
ENST00000394236.9:c.*98G= MANE Select ENSP00000377783.3:n.*98G=
ENST00000407433.6:c.*98G= ENSP00000385794.2:n.*98G=
ENST00000647936.1:c.*232G= ENSP00000496822.1:n.*232G=
ENST00000648381.1:n.2297G=
ENST00000648853.1:c.*98G= ENSP00000497262.1:n.*98G=
ENST00000650591.1:c.*98G= ENSP00000497376.1:n.*98G=
ENST00000394236.7:c.*98G= ENSP00000377783.3:n.*98G=
ENST00000407433.5:c.*98G= ENSP00000385794.1:n.*98G=
NM_000313.3:c.*98G= , LRG_572t1:c.*98G= NP_000304.2:n.*98G=
NM_001314077.1:c.*98G= , LRG_572t2:c.*98G= NP_001301006.1:n.*98G=
NM_000313.4:c.*98G= MANE Select NP_000304.2:n.*98G=
NM_001314077.2:c.*98G= NP_001301006.1:n.*98G=