Canonical Allele Identifier: CA2757500403

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874105_93874111del , CM000665.2:g.93874105_93874111del	GRCh38
NC_000003.11:g.93592949_93592955del , CM000665.1:g.93592949_93592955del	GRCh37
NC_000003.10:g.95075639_95075645del	NCBI36
NG_009813.1:g.104983_104989del , LRG_572:g.104983_104989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+136_*1+142del	ENSP00000330021.7:n.*1+136_*1+142del
ENST00000394236.9:c.*137_*143del MANE Select	ENSP00000377783.3:n.*137_*143del
ENST00000407433.6:c.*137_*143del	ENSP00000385794.2:n.*137_*143del
ENST00000647936.1:c.*271_*277del	ENSP00000496822.1:n.*271_*277del
ENST00000648381.1:n.2336_2342del
ENST00000648853.1:c.*137_*143del	ENSP00000497262.1:n.*137_*143del
ENST00000650591.1:c.*137_*143del	ENSP00000497376.1:n.*137_*143del
ENST00000394236.7:c.*137_*143del	ENSP00000377783.3:n.*137_*143del
ENST00000407433.5:c.*137_*143del	ENSP00000385794.1:n.*137_*143del
NM_000313.3:c.*137_*143del , LRG_572t1:c.*137_*143del	NP_000304.2:n.*137_*143del
NM_001314077.1:c.*137_*143del , LRG_572t2:c.*137_*143del	NP_001301006.1:n.*137_*143del
NM_000313.4:c.*137_*143del MANE Select	NP_000304.2:n.*137_*143del
NM_001314077.2:c.*137_*143del	NP_001301006.1:n.*137_*143del