Canonical Allele Identifier: CA2666653124
Gene: PROS1 HGNC NCBI

Linked Data

gnomAD v4: 3-93874174-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874174C>G , CM000665.2:g.93874174C>G GRCh38
NC_000003.11:g.93593018C>G , CM000665.1:g.93593018C>G GRCh37
NC_000003.10:g.95075708C>G NCBI36
NG_009813.1:g.104917G>C , LRG_572:g.104917G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+70G>C ENSP00000330021.7:n.*1+70G>C
ENST00000394236.9:c.*71G>C MANE Select ENSP00000377783.3:n.*71G>C
ENST00000407433.6:c.*71G>C ENSP00000385794.2:n.*71G>C
ENST00000647936.1:c.*205G>C ENSP00000496822.1:n.*205G>C
ENST00000648381.1:n.2270G>C
ENST00000648853.1:c.*71G>C ENSP00000497262.1:n.*71G>C
ENST00000650591.1:c.*71G>C ENSP00000497376.1:n.*71G>C
ENST00000394236.7:c.*71G>C ENSP00000377783.3:n.*71G>C
ENST00000407433.5:c.*71G>C ENSP00000385794.1:n.*71G>C
NM_000313.3:c.*71G>C , LRG_572t1:c.*71G>C NP_000304.2:n.*71G>C
NM_001314077.1:c.*71G>C , LRG_572t2:c.*71G>C NP_001301006.1:n.*71G>C
NM_000313.4:c.*71G>C MANE Select NP_000304.2:n.*71G>C
NM_001314077.2:c.*71G>C NP_001301006.1:n.*71G>C
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