Canonical Allele Identifier: CA2666653118
Gene: PROS1 HGNC NCBI

Linked Data

gnomAD v4: 3-93874146-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874146T>G , CM000665.2:g.93874146T>G GRCh38
NC_000003.11:g.93592990T>G , CM000665.1:g.93592990T>G GRCh37
NC_000003.10:g.95075680T>G NCBI36
NG_009813.1:g.104945A>C , LRG_572:g.104945A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+98A>C ENSP00000330021.7:n.*1+98A>C
ENST00000394236.9:c.*99A>C MANE Select ENSP00000377783.3:n.*99A>C
ENST00000407433.6:c.*99A>C ENSP00000385794.2:n.*99A>C
ENST00000647936.1:c.*233A>C ENSP00000496822.1:n.*233A>C
ENST00000648381.1:n.2298A>C
ENST00000648853.1:c.*99A>C ENSP00000497262.1:n.*99A>C
ENST00000650591.1:c.*99A>C ENSP00000497376.1:n.*99A>C
ENST00000394236.7:c.*99A>C ENSP00000377783.3:n.*99A>C
ENST00000407433.5:c.*99A>C ENSP00000385794.1:n.*99A>C
NM_000313.3:c.*99A>C , LRG_572t1:c.*99A>C NP_000304.2:n.*99A>C
NM_001314077.1:c.*99A>C , LRG_572t2:c.*99A>C NP_001301006.1:n.*99A>C
NM_000313.4:c.*99A>C MANE Select NP_000304.2:n.*99A>C
NM_001314077.2:c.*99A>C NP_001301006.1:n.*99A>C
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