Canonical Allele Identifier: CA1385026914
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874294A= , CM000665.2:g.93874294A= GRCh38
NC_000003.11:g.93593138A= , CM000665.1:g.93593138A= GRCh37
NC_000003.10:g.95075828A= NCBI36
NG_009813.1:g.104797T= , LRG_572:g.104797T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1982T= ENSP00000330021.7:p.Ile661=
ENST00000394236.9:c.1982T= MANE Select ENSP00000377783.3:p.Ile661=
ENST00000407433.6:c.1937T= ENSP00000385794.2:p.Ile646=
ENST00000647936.1:c.*85T= ENSP00000496822.1:n.*85T=
ENST00000648381.1:n.2150T=
ENST00000648853.1:c.1940T= ENSP00000497262.1:p.Ile647=
ENST00000650591.1:c.2078T= ENSP00000497376.1:p.Ile693=
ENST00000394236.7:c.1982T= ENSP00000377783.3:p.Ile661=
ENST00000407433.5:c.1589T= ENSP00000385794.1:p.Ile530=
NM_000313.3:c.1982T= , LRG_572t1:c.1982T= NP_000304.2:p.Ile661=
NM_001314077.1:c.2078T= , LRG_572t2:c.2078T= NP_001301006.1:p.Ile693=
NM_000313.4:c.1982T= MANE Select NP_000304.2:p.Ile661=
NM_001314077.2:c.2078T= NP_001301006.1:p.Ile693=