Canonical Allele Identifier: CA2666653146

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874238-A-AGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874240_93874242dup , CM000665.2:g.93874240_93874242dup	GRCh38
NC_000003.11:g.93593084_93593086dup , CM000665.1:g.93593084_93593086dup	GRCh37
NC_000003.10:g.95075774_95075776dup	NCBI36
NG_009813.1:g.104850_104852dup , LRG_572:g.104850_104852dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+3_*1+5dup	ENSP00000330021.7:n.*1+3_*1+5dup
ENST00000394236.9:c.*4_*6dup MANE Select	ENSP00000377783.3:n.*4_*6dup
ENST00000407433.6:c.*4_*6dup	ENSP00000385794.2:n.*4_*6dup
ENST00000647936.1:c.*138_*140dup	ENSP00000496822.1:n.*138_*140dup
ENST00000648381.1:n.2203_2205dup
ENST00000648853.1:c.*4_*6dup	ENSP00000497262.1:n.*4_*6dup
ENST00000650591.1:c.*4_*6dup	ENSP00000497376.1:n.*4_*6dup
ENST00000394236.7:c.*4_*6dup	ENSP00000377783.3:n.*4_*6dup
ENST00000407433.5:c.*4_*6dup	ENSP00000385794.1:n.*4_*6dup
NM_000313.3:c.*4_*6dup , LRG_572t1:c.*4_*6dup	NP_000304.2:n.*4_*6dup
NM_001314077.1:c.*4_*6dup , LRG_572t2:c.*4_*6dup	NP_001301006.1:n.*4_*6dup
NM_000313.4:c.*4_*6dup MANE Select	NP_000304.2:n.*4_*6dup
NM_001314077.2:c.*4_*6dup	NP_001301006.1:n.*4_*6dup