Canonical Allele Identifier: CA2666657113

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896783-TTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896786_93896788del , CM000665.2:g.93896786_93896788del	GRCh38
NC_000003.11:g.93615630_93615632del , CM000665.1:g.93615630_93615632del	GRCh37
NC_000003.10:g.95098320_95098322del	NCBI36
NG_009813.1:g.82305_82307del , LRG_572:g.82305_82307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.850-95_850-93del	ENSP00000330021.7:n.850-95_850-93del
ENST00000394236.9:c.850-95_850-93del MANE Select	ENSP00000377783.3:n.850-95_850-93del
ENST00000407433.6:c.805-95_805-93del	ENSP00000385794.2:n.805-95_805-93del
ENST00000647936.1:c.850-95_850-93del	ENSP00000496822.1:n.850-95_850-93del
ENST00000648381.1:n.1018-95_1018-93del
ENST00000648853.1:c.808-95_808-93del	ENSP00000497262.1:n.808-95_808-93del
ENST00000649103.1:c.949-95_949-93del	ENSP00000497962.1:n.949-95_949-93del
ENST00000650591.1:c.946-95_946-93del	ENSP00000497376.1:n.946-95_946-93del
ENST00000394236.7:c.850-95_850-93del	ENSP00000377783.3:n.850-95_850-93del
ENST00000407433.5:c.457-95_457-93del	ENSP00000385794.1:n.457-95_457-93del
NM_000313.3:c.850-95_850-93del , LRG_572t1:c.850-95_850-93del	NP_000304.2:n.850-95_850-93del
NM_001314077.1:c.946-95_946-93del , LRG_572t2:c.946-95_946-93del	NP_001301006.1:n.946-95_946-93del
NM_000313.4:c.850-95_850-93del MANE Select	NP_000304.2:n.850-95_850-93del
NM_001314077.2:c.946-95_946-93del	NP_001301006.1:n.946-95_946-93del