Canonical Allele Identifier: CA1385040060
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93900547_93900550delinsTACC , CM000665.2:g.93900547_93900550delinsTACC GRCh38
NC_000003.11:g.93619391_93619394delinsTACC , CM000665.1:g.93619391_93619394delinsTACC GRCh37
NC_000003.10:g.95102081_95102084delinsTACC NCBI36
NG_009813.1:g.78541_78544delinsGGTA , LRG_572:g.78541_78544delinsGGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.727+254_727+257delinsGGTA ENSP00000330021.7:n.727+254_727+257delinsGGTA
ENST00000394236.9:c.727+254_727+257delinsGGTA MANE Select ENSP00000377783.3:n.727+254_727+257delinsGGTA
ENST00000407433.6:c.682+254_682+257delinsGGTA ENSP00000385794.2:n.682+254_682+257delinsGGTA
ENST00000647936.1:c.727+254_727+257delinsGGTA ENSP00000496822.1:n.727+254_727+257delinsGGTA
ENST00000648381.1:n.895+254_895+257delinsGGTA
ENST00000648853.1:c.685+254_685+257delinsGGTA ENSP00000497262.1:n.685+254_685+257delinsGGTA
ENST00000649103.1:c.826+254_826+257delinsGGTA ENSP00000497962.1:n.826+254_826+257delinsGGTA
ENST00000650591.1:c.823+254_823+257delinsGGTA ENSP00000497376.1:n.823+254_823+257delinsGGTA
ENST00000394236.7:c.727+254_727+257delinsGGTA ENSP00000377783.3:n.727+254_727+257delinsGGTA
ENST00000407433.5:c.334+254_334+257delinsGGTA ENSP00000385794.1:n.334+254_334+257delinsGGTA
NM_000313.3:c.727+254_727+257delinsGGTA , LRG_572t1:c.727+254_727+257delinsGGTA NP_000304.2:n.727+254_727+257delinsGGTA
NM_001314077.1:c.823+254_823+257delinsGGTA , LRG_572t2:c.823+254_823+257delinsGGTA NP_001301006.1:n.823+254_823+257delinsGGTA
NM_000313.4:c.727+254_727+257delinsGGTA MANE Select NP_000304.2:n.727+254_727+257delinsGGTA
NM_001314077.2:c.823+254_823+257delinsGGTA NP_001301006.1:n.823+254_823+257delinsGGTA