Canonical Allele Identifier: CA2666657351

Gene: PROS1

Linked Data

• gnomAD v4: 3-93900792-CCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900797_93900799del , CM000665.2:g.93900797_93900799del	GRCh38
NC_000003.11:g.93619641_93619643del , CM000665.1:g.93619641_93619643del	GRCh37
NC_000003.10:g.95102331_95102333del	NCBI36
NG_009813.1:g.78296_78298del , LRG_572:g.78296_78298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+9_727+11del	ENSP00000330021.7:n.727+9_727+11del
ENST00000394236.9:c.727+9_727+11del MANE Select	ENSP00000377783.3:n.727+9_727+11del
ENST00000407433.6:c.682+9_682+11del	ENSP00000385794.2:n.682+9_682+11del
ENST00000647936.1:c.727+9_727+11del	ENSP00000496822.1:n.727+9_727+11del
ENST00000648381.1:n.895+9_895+11del
ENST00000648853.1:c.685+9_685+11del	ENSP00000497262.1:n.685+9_685+11del
ENST00000649103.1:c.826+9_826+11del	ENSP00000497962.1:n.826+9_826+11del
ENST00000650591.1:c.823+9_823+11del	ENSP00000497376.1:n.823+9_823+11del
ENST00000394236.7:c.727+9_727+11del	ENSP00000377783.3:n.727+9_727+11del
ENST00000407433.5:c.334+9_334+11del	ENSP00000385794.1:n.334+9_334+11del
NM_000313.3:c.727+9_727+11del , LRG_572t1:c.727+9_727+11del	NP_000304.2:n.727+9_727+11del
NM_001314077.1:c.823+9_823+11del , LRG_572t2:c.823+9_823+11del	NP_001301006.1:n.823+9_823+11del
NM_000313.4:c.727+9_727+11del MANE Select	NP_000304.2:n.727+9_727+11del
NM_001314077.2:c.823+9_823+11del	NP_001301006.1:n.823+9_823+11del