Canonical Allele Identifier: CA912658148

Gene: PROS1

Linked Data

• dbSNP Id: rs1340202479
• MyVariant Identifiers: chr3:g.93627716_93627734del (hg19) ; chr3:g.93908872_93908890del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93908872_93908890del , CM000665.2:g.93908872_93908890del	GRCh38
NC_000003.11:g.93627716_93627734del , CM000665.1:g.93627716_93627734del	GRCh37
NC_000003.10:g.95110406_95110424del	NCBI36
NG_009813.1:g.70201_70219del , LRG_572:g.70201_70219del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.346+1729_346+1747del	ENSP00000330021.7:n.346+1729_346+1747del
ENST00000394236.9:c.346+1729_346+1747del MANE Select	ENSP00000377783.3:n.346+1729_346+1747del
ENST00000407433.6:c.346+1729_346+1747del	ENSP00000385794.2:n.346+1729_346+1747del
ENST00000472684.2:c.-48+1729_-48+1747del	ENSP00000419616.2:n.-48+1729_-48+1747del
ENST00000647936.1:c.346+1729_346+1747del	ENSP00000496822.1:n.346+1729_346+1747del
ENST00000648381.1:n.514+1729_514+1747del
ENST00000648853.1:c.304+1729_304+1747del	ENSP00000497262.1:n.304+1729_304+1747del
ENST00000649103.1:c.445+1729_445+1747del	ENSP00000497962.1:n.445+1729_445+1747del
ENST00000650591.1:c.442+1729_442+1747del	ENSP00000497376.1:n.442+1729_442+1747del
ENST00000348974.4:c.442+1729_442+1747del	ENSP00000330021.6:n.442+1729_442+1747del
ENST00000394236.7:c.346+1729_346+1747del	ENSP00000377783.3:n.346+1729_346+1747del
ENST00000407433.5:c.-48+1729_-48+1747del	ENSP00000385794.1:n.-48+1729_-48+1747del
ENST00000472684.1:c.-48+1729_-48+1747del	ENSP00000419616.1:n.-48+1729_-48+1747del
ENST00000488658.1:n.539+1729_539+1747del
NM_000313.3:c.346+1729_346+1747del , LRG_572t1:c.346+1729_346+1747del	NP_000304.2:n.346+1729_346+1747del
NM_001314077.1:c.442+1729_442+1747del , LRG_572t2:c.442+1729_442+1747del	NP_001301006.1:n.442+1729_442+1747del
NM_000313.4:c.346+1729_346+1747del MANE Select	NP_000304.2:n.346+1729_346+1747del
NM_001314077.2:c.442+1729_442+1747del	NP_001301006.1:n.442+1729_442+1747del