Canonical Allele Identifier: CA1385026781
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93873968_93873969delinsCA , CM000665.2:g.93873968_93873969delinsCA GRCh38
NC_000003.11:g.93592812_93592813delinsCA , CM000665.1:g.93592812_93592813delinsCA GRCh37
NC_000003.10:g.95075502_95075503delinsCA NCBI36
NG_009813.1:g.105122_105123delinsTG , LRG_572:g.105122_105123delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.*1+275_*1+276delinsTG ENSP00000330021.7:n.*1+275_*1+276delinsTG
ENST00000394236.9:c.*276_*277delinsTG MANE Select ENSP00000377783.3:n.*276_*277delinsTG
ENST00000407433.6:c.*276_*277delinsTG ENSP00000385794.2:n.*276_*277delinsTG
ENST00000647936.1:c.*410_*411delinsTG ENSP00000496822.1:n.*410_*411delinsTG
ENST00000648381.1:n.2475_2476delinsTG
ENST00000648853.1:c.*276_*277delinsTG ENSP00000497262.1:n.*276_*277delinsTG
ENST00000650591.1:c.*276_*277delinsTG ENSP00000497376.1:n.*276_*277delinsTG
ENST00000394236.7:c.*276_*277delinsTG ENSP00000377783.3:n.*276_*277delinsTG
ENST00000407433.5:c.*276_*277delinsTG ENSP00000385794.1:n.*276_*277delinsTG
NM_000313.3:c.*276_*277delinsTG , LRG_572t1:c.*276_*277delinsTG NP_000304.2:n.*276_*277delinsTG
NM_001314077.1:c.*276_*277delinsTG , LRG_572t2:c.*276_*277delinsTG NP_001301006.1:n.*276_*277delinsTG
NM_000313.4:c.*276_*277delinsTG MANE Select NP_000304.2:n.*276_*277delinsTG
NM_001314077.2:c.*276_*277delinsTG NP_001301006.1:n.*276_*277delinsTG