Canonical Allele Identifier: CA2666653143

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874230-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874231del , CM000665.2:g.93874231del	GRCh38
NC_000003.11:g.93593075del , CM000665.1:g.93593075del	GRCh37
NC_000003.10:g.95075765del	NCBI36
NG_009813.1:g.104860del , LRG_572:g.104860del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+13del	ENSP00000330021.7:n.*1+13del
ENST00000394236.9:c.*14del MANE Select	ENSP00000377783.3:n.*14del
ENST00000407433.6:c.*14del	ENSP00000385794.2:n.*14del
ENST00000647936.1:c.*148del	ENSP00000496822.1:n.*148del
ENST00000648381.1:n.2213del
ENST00000648853.1:c.*14del	ENSP00000497262.1:n.*14del
ENST00000650591.1:c.*14del	ENSP00000497376.1:n.*14del
ENST00000394236.7:c.*14del	ENSP00000377783.3:n.*14del
ENST00000407433.5:c.*14del	ENSP00000385794.1:n.*14del
NM_000313.3:c.*14del , LRG_572t1:c.*14del	NP_000304.2:n.*14del
NM_001314077.1:c.*14del , LRG_572t2:c.*14del	NP_001301006.1:n.*14del
NM_000313.4:c.*14del MANE Select	NP_000304.2:n.*14del
NM_001314077.2:c.*14del	NP_001301006.1:n.*14del