Canonical Allele Identifier: CA544751919
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1388500391

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905443dup , CM000665.2:g.93905443dup GRCh38
NC_000003.11:g.93624287dup , CM000665.1:g.93624287dup GRCh37
NC_000003.10:g.95106977dup NCBI36
NG_009813.1:g.73653dup , LRG_572:g.73653dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.601+346dup ENSP00000330021.7:n.601+346dup
ENST00000394236.9:c.601+346dup MANE Select ENSP00000377783.3:n.601+346dup
ENST00000407433.6:c.556+391dup ENSP00000385794.2:n.556+391dup
ENST00000647936.1:c.601+346dup ENSP00000496822.1:n.601+346dup
ENST00000648381.1:n.769+346dup
ENST00000648853.1:c.559+346dup ENSP00000497262.1:n.559+346dup
ENST00000649103.1:c.700+346dup ENSP00000497962.1:n.700+346dup
ENST00000650591.1:c.697+346dup ENSP00000497376.1:n.697+346dup
ENST00000394236.7:c.601+346dup ENSP00000377783.3:n.601+346dup
ENST00000407433.5:c.208+346dup ENSP00000385794.1:n.208+346dup
NM_000313.3:c.601+346dup , LRG_572t1:c.601+346dup NP_000304.2:n.601+346dup
NM_001314077.1:c.697+346dup , LRG_572t2:c.697+346dup NP_001301006.1:n.697+346dup
NM_000313.4:c.601+346dup MANE Select NP_000304.2:n.601+346dup
NM_001314077.2:c.697+346dup NP_001301006.1:n.697+346dup