Canonical Allele Identifier: CA353667804
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93884779T>C , CM000665.2:g.93884779T>C GRCh38
NC_000003.11:g.93603623T>C , CM000665.1:g.93603623T>C GRCh37
NC_000003.10:g.95086313T>C NCBI36
NG_009813.1:g.94312A>G , LRG_572:g.94312A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1441A>G ENSP00000330021.7:p.Lys481Glu
ENST00000394236.9:c.1441A>G MANE Select ENSP00000377783.3:p.Lys481Glu
ENST00000407433.6:c.1396A>G ENSP00000385794.2:p.Lys466Glu
ENST00000647936.1:c.1441A>G ENSP00000496822.1:p.Lys481Glu
ENST00000648381.1:n.1609A>G
ENST00000648853.1:c.1399A>G ENSP00000497262.1:p.Lys467Glu
ENST00000649103.1:c.1540A>G ENSP00000497962.1:n.1540A>G
ENST00000649585.1:c.196A>G ENSP00000498163.1:p.Lys66Glu
ENST00000650591.1:c.1537A>G ENSP00000497376.1:p.Lys513Glu
ENST00000394236.7:c.1441A>G ENSP00000377783.3:p.Lys481Glu
ENST00000407433.5:c.1048A>G ENSP00000385794.1:p.Lys350Glu
NM_000313.3:c.1441A>G , LRG_572t1:c.1441A>G NP_000304.2:p.Lys481Glu
NM_001314077.1:c.1537A>G , LRG_572t2:c.1537A>G NP_001301006.1:p.Lys513Glu
NM_000313.4:c.1441A>G MANE Select NP_000304.2:p.Lys481Glu
NM_001314077.2:c.1537A>G NP_001301006.1:p.Lys513Glu