Canonical Allele Identifier: CA1385038306
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896608T= , CM000665.2:g.93896608T= GRCh38
NC_000003.11:g.93615452T= , CM000665.1:g.93615452T= GRCh37
NC_000003.10:g.95098142T= NCBI36
NG_009813.1:g.82483A= , LRG_572:g.82483A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.933A= ENSP00000330021.7:p.Leu311=
ENST00000394236.9:c.933A= MANE Select ENSP00000377783.3:p.Leu311=
ENST00000407433.6:c.888A= ENSP00000385794.2:p.Leu296=
ENST00000647936.1:c.933A= ENSP00000496822.1:p.Leu311=
ENST00000648381.1:n.1101A=
ENST00000648853.1:c.891A= ENSP00000497262.1:p.Leu297=
ENST00000649103.1:c.1032A= ENSP00000497962.1:n.1032A=
ENST00000650591.1:c.1029A= ENSP00000497376.1:p.Leu343=
ENST00000394236.7:c.933A= ENSP00000377783.3:p.Leu311=
ENST00000407433.5:c.540A= ENSP00000385794.1:p.Leu180=
NM_000313.3:c.933A= , LRG_572t1:c.933A= NP_000304.2:p.Leu311=
NM_001314077.1:c.1029A= , LRG_572t2:c.1029A= NP_001301006.1:p.Leu343=
NM_000313.4:c.933A= MANE Select NP_000304.2:p.Leu311=
NM_001314077.2:c.1029A= NP_001301006.1:p.Leu343=