Canonical Allele Identifier: CA2666657348

Gene: PROS1

Linked Data

• gnomAD v4: 3-93900787-TACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900792_93900794del , CM000665.2:g.93900792_93900794del	GRCh38
NC_000003.11:g.93619636_93619638del , CM000665.1:g.93619636_93619638del	GRCh37
NC_000003.10:g.95102326_95102328del	NCBI36
NG_009813.1:g.78301_78303del , LRG_572:g.78301_78303del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+14_727+16del	ENSP00000330021.7:n.727+14_727+16del
ENST00000394236.9:c.727+14_727+16del MANE Select	ENSP00000377783.3:n.727+14_727+16del
ENST00000407433.6:c.682+14_682+16del	ENSP00000385794.2:n.682+14_682+16del
ENST00000647936.1:c.727+14_727+16del	ENSP00000496822.1:n.727+14_727+16del
ENST00000648381.1:n.895+14_895+16del
ENST00000648853.1:c.685+14_685+16del	ENSP00000497262.1:n.685+14_685+16del
ENST00000649103.1:c.826+14_826+16del	ENSP00000497962.1:n.826+14_826+16del
ENST00000650591.1:c.823+14_823+16del	ENSP00000497376.1:n.823+14_823+16del
ENST00000394236.7:c.727+14_727+16del	ENSP00000377783.3:n.727+14_727+16del
ENST00000407433.5:c.334+14_334+16del	ENSP00000385794.1:n.334+14_334+16del
NM_000313.3:c.727+14_727+16del , LRG_572t1:c.727+14_727+16del	NP_000304.2:n.727+14_727+16del
NM_001314077.1:c.823+14_823+16del , LRG_572t2:c.823+14_823+16del	NP_001301006.1:n.823+14_823+16del
NM_000313.4:c.727+14_727+16del MANE Select	NP_000304.2:n.727+14_727+16del
NM_001314077.2:c.823+14_823+16del	NP_001301006.1:n.823+14_823+16del