Canonical Allele Identifier: CA1385026613
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93873740_93873741delinsTG , CM000665.2:g.93873740_93873741delinsTG GRCh38
NC_000003.11:g.93592584_93592585delinsTG , CM000665.1:g.93592584_93592585delinsTG GRCh37
NC_000003.10:g.95075274_95075275delinsTG NCBI36
NG_009813.1:g.105350_105351delinsCA , LRG_572:g.105350_105351delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.*2-328_*2-327delinsCA ENSP00000330021.7:n.*2-328_*2-327delinsCA
ENST00000394236.9:c.*504_*505delinsCA MANE Select ENSP00000377783.3:n.*504_*505delinsCA
ENST00000407433.6:c.*504_*505delinsCA ENSP00000385794.2:n.*504_*505delinsCA
ENST00000647936.1:c.*638_*639delinsCA ENSP00000496822.1:n.*638_*639delinsCA
ENST00000648381.1:n.2703_2704delinsCA
ENST00000648853.1:c.*504_*505delinsCA ENSP00000497262.1:n.*504_*505delinsCA
ENST00000650591.1:c.*504_*505delinsCA ENSP00000497376.1:n.*504_*505delinsCA
ENST00000394236.7:c.*504_*505delinsCA ENSP00000377783.3:n.*504_*505delinsCA
ENST00000407433.5:c.*504_*505delinsCA ENSP00000385794.1:n.*504_*505delinsCA
NM_000313.3:c.*504_*505delinsCA , LRG_572t1:c.*504_*505delinsCA NP_000304.2:n.*504_*505delinsCA
NM_001314077.1:c.*504_*505delinsCA , LRG_572t2:c.*504_*505delinsCA NP_001301006.1:n.*504_*505delinsCA
NM_000313.4:c.*504_*505delinsCA MANE Select NP_000304.2:n.*504_*505delinsCA
NM_001314077.2:c.*504_*505delinsCA NP_001301006.1:n.*504_*505delinsCA