Canonical Allele Identifier: CA2571157314

Gene: PROS1

Linked Data

• gnomAD v4: 3-93873767-CCATTCAATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873771_93873779del , CM000665.2:g.93873771_93873779del	GRCh38
NC_000003.11:g.93592615_93592623del , CM000665.1:g.93592615_93592623del	GRCh37
NC_000003.10:g.95075305_95075313del	NCBI36
NG_009813.1:g.105315_105323del , LRG_572:g.105315_105323del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-363_*2-355del	ENSP00000330021.7:n.*2-363_*2-355del
ENST00000394236.9:c.*469_*477del MANE Select	ENSP00000377783.3:n.*469_*477del
ENST00000407433.6:c.*469_*477del	ENSP00000385794.2:n.*469_*477del
ENST00000647936.1:c.*603_*611del	ENSP00000496822.1:n.*603_*611del
ENST00000648381.1:n.2668_2676del
ENST00000648853.1:c.*469_*477del	ENSP00000497262.1:n.*469_*477del
ENST00000650591.1:c.*469_*477del	ENSP00000497376.1:n.*469_*477del
ENST00000394236.7:c.*469_*477del	ENSP00000377783.3:n.*469_*477del
ENST00000407433.5:c.*469_*477del	ENSP00000385794.1:n.*469_*477del
NM_000313.3:c.*469_*477del , LRG_572t1:c.*469_*477del	NP_000304.2:n.*469_*477del
NM_001314077.1:c.*469_*477del , LRG_572t2:c.*469_*477del	NP_001301006.1:n.*469_*477del
NM_000313.4:c.*469_*477del MANE Select	NP_000304.2:n.*469_*477del
NM_001314077.2:c.*469_*477del	NP_001301006.1:n.*469_*477del