Canonical Allele Identifier: CA2666652954

Gene: PROS1

Linked Data

• gnomAD v4: 3-93873830-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873831del , CM000665.2:g.93873831del	GRCh38
NC_000003.11:g.93592675del , CM000665.1:g.93592675del	GRCh37
NC_000003.10:g.95075365del	NCBI36
NG_009813.1:g.105260del , LRG_572:g.105260del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+413del	ENSP00000330021.7:n.*1+413del
ENST00000394236.9:c.*414del MANE Select	ENSP00000377783.3:n.*414del
ENST00000407433.6:c.*414del	ENSP00000385794.2:n.*414del
ENST00000647936.1:c.*548del	ENSP00000496822.1:n.*548del
ENST00000648381.1:n.2613del
ENST00000648853.1:c.*414del	ENSP00000497262.1:n.*414del
ENST00000650591.1:c.*414del	ENSP00000497376.1:n.*414del
ENST00000394236.7:c.*414del	ENSP00000377783.3:n.*414del
ENST00000407433.5:c.*414del	ENSP00000385794.1:n.*414del
NM_000313.3:c.*414del , LRG_572t1:c.*414del	NP_000304.2:n.*414del
NM_001314077.1:c.*414del , LRG_572t2:c.*414del	NP_001301006.1:n.*414del
NM_000313.4:c.*414del MANE Select	NP_000304.2:n.*414del
NM_001314077.2:c.*414del	NP_001301006.1:n.*414del