Canonical Allele Identifier: CA2666653151

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874244-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874246dup , CM000665.2:g.93874246dup	GRCh38
NC_000003.11:g.93593090dup , CM000665.1:g.93593090dup	GRCh37
NC_000003.10:g.95075780dup	NCBI36
NG_009813.1:g.104846dup , LRG_572:g.104846dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.2031dup	ENSP00000330021.7:n.2031dup
ENST00000394236.9:c.2031dup MANE Select	ENSP00000377783.3:n.2031dup
ENST00000407433.6:c.1986dup	ENSP00000385794.2:n.1986dup
ENST00000647936.1:c.*134dup	ENSP00000496822.1:n.*134dup
ENST00000648381.1:n.2199dup
ENST00000648853.1:c.1989dup	ENSP00000497262.1:n.1989dup
ENST00000650591.1:c.2127dup	ENSP00000497376.1:n.2127dup
ENST00000394236.7:c.2031dup	ENSP00000377783.3:n.2031dup
ENST00000407433.5:c.1638dup	ENSP00000385794.1:n.1638dup
NM_000313.3:c.2031dup , LRG_572t1:c.2031dup	NP_000304.2:n.2031dup
NM_001314077.1:c.2127dup , LRG_572t2:c.2127dup	NP_001301006.1:n.2127dup
NM_000313.4:c.2031dup MANE Select	NP_000304.2:n.2031dup
NM_001314077.2:c.2127dup	NP_001301006.1:n.2127dup