Canonical Allele Identifier: CA1385026710

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873835_93873836delinsCA , CM000665.2:g.93873835_93873836delinsCA	GRCh38
NC_000003.11:g.93592679_93592680delinsCA , CM000665.1:g.93592679_93592680delinsCA	GRCh37
NC_000003.10:g.95075369_95075370delinsCA	NCBI36
NG_009813.1:g.105255_105256delinsTG , LRG_572:g.105255_105256delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+408_*1+409delinsTG	ENSP00000330021.7:n.*1+408_*1+409delinsTG
ENST00000394236.9:c.*409_*410delinsTG MANE Select	ENSP00000377783.3:n.*409_*410delinsTG
ENST00000407433.6:c.*409_*410delinsTG	ENSP00000385794.2:n.*409_*410delinsTG
ENST00000647936.1:c.*543_*544delinsTG	ENSP00000496822.1:n.*543_*544delinsTG
ENST00000648381.1:n.2608_2609delinsTG
ENST00000648853.1:c.*409_*410delinsTG	ENSP00000497262.1:n.*409_*410delinsTG
ENST00000650591.1:c.*409_*410delinsTG	ENSP00000497376.1:n.*409_*410delinsTG
ENST00000394236.7:c.*409_*410delinsTG	ENSP00000377783.3:n.*409_*410delinsTG
ENST00000407433.5:c.*409_*410delinsTG	ENSP00000385794.1:n.*409_*410delinsTG
NM_000313.3:c.*409_*410delinsTG , LRG_572t1:c.*409_*410delinsTG	NP_000304.2:n.*409_*410delinsTG
NM_001314077.1:c.*409_*410delinsTG , LRG_572t2:c.*409_*410delinsTG	NP_001301006.1:n.*409_*410delinsTG
NM_000313.4:c.*409_*410delinsTG MANE Select	NP_000304.2:n.*409_*410delinsTG
NM_001314077.2:c.*409_*410delinsTG	NP_001301006.1:n.*409_*410delinsTG