Canonical Allele Identifier: CA1385038301
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896599T= , CM000665.2:g.93896599T= GRCh38
NC_000003.11:g.93615443T= , CM000665.1:g.93615443T= GRCh37
NC_000003.10:g.95098133T= NCBI36
NG_009813.1:g.82492A= , LRG_572:g.82492A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.942A= ENSP00000330021.7:p.Lys314=
ENST00000394236.9:c.942A= MANE Select ENSP00000377783.3:p.Lys314=
ENST00000407433.6:c.897A= ENSP00000385794.2:p.Lys299=
ENST00000647936.1:c.942A= ENSP00000496822.1:p.Lys314=
ENST00000648381.1:n.1110A=
ENST00000648853.1:c.900A= ENSP00000497262.1:p.Lys300=
ENST00000649103.1:c.1041A= ENSP00000497962.1:n.1041A=
ENST00000650591.1:c.1038A= ENSP00000497376.1:p.Lys346=
ENST00000394236.7:c.942A= ENSP00000377783.3:p.Lys314=
ENST00000407433.5:c.549A= ENSP00000385794.1:p.Lys183=
NM_000313.3:c.942A= , LRG_572t1:c.942A= NP_000304.2:p.Lys314=
NM_001314077.1:c.1038A= , LRG_572t2:c.1038A= NP_001301006.1:p.Lys346=
NM_000313.4:c.942A= MANE Select NP_000304.2:p.Lys314=
NM_001314077.2:c.1038A= NP_001301006.1:p.Lys346=