Canonical Allele Identifier: CA2577828409

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900774_93900776del , CM000665.2:g.93900774_93900776del	GRCh38
NC_000003.11:g.93619618_93619620del , CM000665.1:g.93619618_93619620del	GRCh37
NC_000003.10:g.95102308_95102310del	NCBI36
NG_009813.1:g.78318_78320del , LRG_572:g.78318_78320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+31_727+33del	ENSP00000330021.7:n.727+31_727+33del
ENST00000394236.9:c.727+31_727+33del MANE Select	ENSP00000377783.3:n.727+31_727+33del
ENST00000407433.6:c.682+31_682+33del	ENSP00000385794.2:n.682+31_682+33del
ENST00000647936.1:c.727+31_727+33del	ENSP00000496822.1:n.727+31_727+33del
ENST00000648381.1:n.895+31_895+33del
ENST00000648853.1:c.685+31_685+33del	ENSP00000497262.1:n.685+31_685+33del
ENST00000649103.1:c.826+31_826+33del	ENSP00000497962.1:n.826+31_826+33del
ENST00000650591.1:c.823+31_823+33del	ENSP00000497376.1:n.823+31_823+33del
ENST00000394236.7:c.727+31_727+33del	ENSP00000377783.3:n.727+31_727+33del
ENST00000407433.5:c.334+31_334+33del	ENSP00000385794.1:n.334+31_334+33del
NM_000313.3:c.727+31_727+33del , LRG_572t1:c.727+31_727+33del	NP_000304.2:n.727+31_727+33del
NM_001314077.1:c.823+31_823+33del , LRG_572t2:c.823+31_823+33del	NP_001301006.1:n.823+31_823+33del
NM_000313.4:c.727+31_727+33del MANE Select	NP_000304.2:n.727+31_727+33del
NM_001314077.2:c.823+31_823+33del	NP_001301006.1:n.823+31_823+33del