Canonical Allele Identifier: CA912683321

Gene: PROS1

Linked Data

• dbSNP Id: rs1292683357
• gnomAD v3: 3-93874090-A-AT
• gnomAD v4: 3-93874090-A-AT
• MyVariant Identifiers: chr3:g.93592934_93592935insT (hg19) ; chr3:g.93874090_93874091insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874097dup , CM000665.2:g.93874097dup	GRCh38
NC_000003.11:g.93592941dup , CM000665.1:g.93592941dup	GRCh37
NC_000003.10:g.95075631dup	NCBI36
NG_009813.1:g.105000dup , LRG_572:g.105000dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+153dup	ENSP00000330021.7:n.*1+153dup
ENST00000394236.9:c.*154dup MANE Select	ENSP00000377783.3:n.*154dup
ENST00000407433.6:c.*154dup	ENSP00000385794.2:n.*154dup
ENST00000647936.1:c.*288dup	ENSP00000496822.1:n.*288dup
ENST00000648381.1:n.2353dup
ENST00000648853.1:c.*154dup	ENSP00000497262.1:n.*154dup
ENST00000650591.1:c.*154dup	ENSP00000497376.1:n.*154dup
ENST00000394236.7:c.*154dup	ENSP00000377783.3:n.*154dup
ENST00000407433.5:c.*154dup	ENSP00000385794.1:n.*154dup
NM_000313.3:c.*154dup , LRG_572t1:c.*154dup	NP_000304.2:n.*154dup
NM_001314077.1:c.*154dup , LRG_572t2:c.*154dup	NP_001301006.1:n.*154dup
NM_000313.4:c.*154dup MANE Select	NP_000304.2:n.*154dup
NM_001314077.2:c.*154dup	NP_001301006.1:n.*154dup