Canonical Allele Identifier: CA1385028846
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93876970A= , CM000665.2:g.93876970A= GRCh38
NC_000003.11:g.93595814A= , CM000665.1:g.93595814A= GRCh37
NC_000003.10:g.95078504A= NCBI36
NG_009813.1:g.102121T= , LRG_572:g.102121T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1866T= ENSP00000330021.7:p.Leu622=
ENST00000394236.9:c.1866T= MANE Select ENSP00000377783.3:p.Leu622=
ENST00000407433.6:c.1821T= ENSP00000385794.2:p.Leu607=
ENST00000647936.1:c.1644+2193T= ENSP00000496822.1:n.1644+2193T=
ENST00000648381.1:n.2034T=
ENST00000648853.1:c.1824T= ENSP00000497262.1:p.Leu608=
ENST00000650591.1:c.1962T= ENSP00000497376.1:p.Leu654=
ENST00000394236.7:c.1866T= ENSP00000377783.3:p.Leu622=
ENST00000407433.5:c.1473T= ENSP00000385794.1:p.Leu491=
NM_000313.3:c.1866T= , LRG_572t1:c.1866T= NP_000304.2:p.Leu622=
NM_001314077.1:c.1962T= , LRG_572t2:c.1962T= NP_001301006.1:p.Leu654=
NM_000313.4:c.1866T= MANE Select NP_000304.2:p.Leu622=
NM_001314077.2:c.1962T= NP_001301006.1:p.Leu654=