Canonical Allele Identifier: CA1050951805

Gene: PROS1

Linked Data

• dbSNP Id: rs1708576959
• gnomAD v3: 3-93900555-A-AAT
• gnomAD v4: 3-93900555-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900555_93900556insAT , CM000665.2:g.93900555_93900556insAT	GRCh38
NC_000003.11:g.93619399_93619400insAT , CM000665.1:g.93619399_93619400insAT	GRCh37
NC_000003.10:g.95102089_95102090insAT	NCBI36
NG_009813.1:g.78535_78536insAT , LRG_572:g.78535_78536insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+248_727+249insAT	ENSP00000330021.7:n.727+248_727+249insAT
ENST00000394236.9:c.727+248_727+249insAT MANE Select	ENSP00000377783.3:n.727+248_727+249insAT
ENST00000407433.6:c.682+248_682+249insAT	ENSP00000385794.2:n.682+248_682+249insAT
ENST00000647936.1:c.727+248_727+249insAT	ENSP00000496822.1:n.727+248_727+249insAT
ENST00000648381.1:n.895+248_895+249insAT
ENST00000648853.1:c.685+248_685+249insAT	ENSP00000497262.1:n.685+248_685+249insAT
ENST00000649103.1:c.826+248_826+249insAT	ENSP00000497962.1:n.826+248_826+249insAT
ENST00000650591.1:c.823+248_823+249insAT	ENSP00000497376.1:n.823+248_823+249insAT
ENST00000394236.7:c.727+248_727+249insAT	ENSP00000377783.3:n.727+248_727+249insAT
ENST00000407433.5:c.334+248_334+249insAT	ENSP00000385794.1:n.334+248_334+249insAT
NM_000313.3:c.727+248_727+249insAT , LRG_572t1:c.727+248_727+249insAT	NP_000304.2:n.727+248_727+249insAT
NM_001314077.1:c.823+248_823+249insAT , LRG_572t2:c.823+248_823+249insAT	NP_001301006.1:n.823+248_823+249insAT
NM_000313.4:c.727+248_727+249insAT MANE Select	NP_000304.2:n.727+248_727+249insAT
NM_001314077.2:c.823+248_823+249insAT	NP_001301006.1:n.823+248_823+249insAT