Canonical Allele Identifier: CA916955747

Gene: PROS1

Linked Data

• dbSNP Id: rs1559933771

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900456_93900459del , CM000665.2:g.93900456_93900459del	GRCh38
NC_000003.11:g.93619300_93619303del , CM000665.1:g.93619300_93619303del	GRCh37
NC_000003.10:g.95101990_95101993del	NCBI36
NG_009813.1:g.78637_78640del , LRG_572:g.78637_78640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+350_727+353del	ENSP00000330021.7:n.727+350_727+353del
ENST00000394236.9:c.727+350_727+353del MANE Select	ENSP00000377783.3:n.727+350_727+353del
ENST00000407433.6:c.682+350_682+353del	ENSP00000385794.2:n.682+350_682+353del
ENST00000647936.1:c.727+350_727+353del	ENSP00000496822.1:n.727+350_727+353del
ENST00000648381.1:n.895+350_895+353del
ENST00000648853.1:c.685+350_685+353del	ENSP00000497262.1:n.685+350_685+353del
ENST00000649103.1:c.826+350_826+353del	ENSP00000497962.1:n.826+350_826+353del
ENST00000650591.1:c.823+350_823+353del	ENSP00000497376.1:n.823+350_823+353del
ENST00000394236.7:c.727+350_727+353del	ENSP00000377783.3:n.727+350_727+353del
ENST00000407433.5:c.334+350_334+353del	ENSP00000385794.1:n.334+350_334+353del
NM_000313.3:c.727+350_727+353del , LRG_572t1:c.727+350_727+353del	NP_000304.2:n.727+350_727+353del
NM_001314077.1:c.823+350_823+353del , LRG_572t2:c.823+350_823+353del	NP_001301006.1:n.823+350_823+353del
NM_000313.4:c.727+350_727+353del MANE Select	NP_000304.2:n.727+350_727+353del
NM_001314077.2:c.823+350_823+353del	NP_001301006.1:n.823+350_823+353del