Canonical Allele Identifier: CA353673398
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905799T>A , CM000665.2:g.93905799T>A GRCh38
NC_000003.11:g.93624643T>A , CM000665.1:g.93624643T>A GRCh37
NC_000003.10:g.95107333T>A NCBI36
NG_009813.1:g.73292A>T , LRG_572:g.73292A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000313.4:c.586A>T MANE Select NP_000304.2:p.Lys196Ter
ENST00000394236.9:c.586A>T MANE Select ENSP00000377783.3:p.Lys196Ter
NM_000313.3:c.586A>T , LRG_572t1:c.586A>T NP_000304.2:p.Lys196Ter
NM_001314077.1:c.682A>T , LRG_572t2:c.682A>T NP_001301006.1:p.Lys228Ter
NM_001314077.2:c.682A>T NP_001301006.1:p.Lys228Ter
ENST00000348974.4:c.682A>T ENSP00000330021.6:p.Lys228Ter
ENST00000348974.5:c.586A>T ENSP00000330021.7:p.Lys196Ter
ENST00000394236.7:c.586A>T ENSP00000377783.3:p.Lys196Ter
ENST00000407433.5:c.193A>T ENSP00000385794.1:p.Lys65Ter
ENST00000407433.6:c.556+30A>T ENSP00000385794.2:n.556+30A>T
ENST00000647936.1:c.586A>T ENSP00000496822.1:p.Lys196Ter
ENST00000648381.1:n.754A>T
ENST00000648853.1:c.544A>T ENSP00000497262.1:p.Lys182Ter
ENST00000649103.1:c.685A>T ENSP00000497962.1:n.685A>T
ENST00000650591.1:c.682A>T ENSP00000497376.1:p.Lys228Ter