Canonical Allele Identifier: CA1385026745

Gene: PROS1

Linked Data

• dbSNP Id: rs1708144627

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873903del , CM000665.2:g.93873903del	GRCh38
NC_000003.11:g.93592747del , CM000665.1:g.93592747del	GRCh37
NC_000003.10:g.95075437del	NCBI36
NG_009813.1:g.105188del , LRG_572:g.105188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+341del	ENSP00000330021.7:n.*1+341del
ENST00000394236.9:c.*342del MANE Select	ENSP00000377783.3:n.*342del
ENST00000407433.6:c.*342del	ENSP00000385794.2:n.*342del
ENST00000647936.1:c.*476del	ENSP00000496822.1:n.*476del
ENST00000648381.1:n.2541del
ENST00000648853.1:c.*342del	ENSP00000497262.1:n.*342del
ENST00000650591.1:c.*342del	ENSP00000497376.1:n.*342del
ENST00000394236.7:c.*342del	ENSP00000377783.3:n.*342del
ENST00000407433.5:c.*342del	ENSP00000385794.1:n.*342del
NM_000313.3:c.*342del , LRG_572t1:c.*342del	NP_000304.2:n.*342del
NM_001314077.1:c.*342del , LRG_572t2:c.*342del	NP_001301006.1:n.*342del
NM_000313.4:c.*342del MANE Select	NP_000304.2:n.*342del
NM_001314077.2:c.*342del	NP_001301006.1:n.*342del