Canonical Allele Identifier: CA353669277
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874247A>T , CM000665.2:g.93874247A>T GRCh38
NC_000003.11:g.93593091A>T , CM000665.1:g.93593091A>T GRCh37
NC_000003.10:g.95075781A>T NCBI36
NG_009813.1:g.104844T>A , LRG_572:g.104844T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.2029T>A ENSP00000330021.7:p.Ter677Lys
ENST00000394236.9:c.2029T>A MANE Select ENSP00000377783.3:p.Ter677Lys
ENST00000407433.6:c.1984T>A ENSP00000385794.2:p.Ter662Lys
ENST00000647936.1:c.*132T>A ENSP00000496822.1:n.*132T>A
ENST00000648381.1:n.2197T>A
ENST00000648853.1:c.1987T>A ENSP00000497262.1:p.Ter663Lys
ENST00000650591.1:c.2125T>A ENSP00000497376.1:p.Ter709Lys
ENST00000394236.7:c.2029T>A ENSP00000377783.3:p.Ter677Lys
ENST00000407433.5:c.1636T>A ENSP00000385794.1:p.Ter546Lys
NM_000313.3:c.2029T>A , LRG_572t1:c.2029T>A NP_000304.2:p.Ter677Lys
NM_001314077.1:c.2125T>A , LRG_572t2:c.2125T>A NP_001301006.1:p.Ter709Lys
NM_000313.4:c.2029T>A MANE Select NP_000304.2:p.Ter677Lys
NM_001314077.2:c.2125T>A NP_001301006.1:p.Ter709Lys