Canonical Allele Identifier: CA912683284

Gene: PROS1

Linked Data

• dbSNP Id: rs1276335756
• gnomAD v4: 3-93874050-GAAGT-G
• MyVariant Identifiers: chr3:g.93592895_93592898del (hg19) ; chr3:g.93874051_93874054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874054_93874057del , CM000665.2:g.93874054_93874057del	GRCh38
NC_000003.11:g.93592898_93592901del , CM000665.1:g.93592898_93592901del	GRCh37
NC_000003.10:g.95075588_95075591del	NCBI36
NG_009813.1:g.105037_105040del , LRG_572:g.105037_105040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+190_*1+193del	ENSP00000330021.7:n.*1+190_*1+193del
ENST00000394236.9:c.*191_*194del MANE Select	ENSP00000377783.3:n.*191_*194del
ENST00000407433.6:c.*191_*194del	ENSP00000385794.2:n.*191_*194del
ENST00000647936.1:c.*325_*328del	ENSP00000496822.1:n.*325_*328del
ENST00000648381.1:n.2390_2393del
ENST00000648853.1:c.*191_*194del	ENSP00000497262.1:n.*191_*194del
ENST00000650591.1:c.*191_*194del	ENSP00000497376.1:n.*191_*194del
ENST00000394236.7:c.*191_*194del	ENSP00000377783.3:n.*191_*194del
ENST00000407433.5:c.*191_*194del	ENSP00000385794.1:n.*191_*194del
NM_000313.3:c.*191_*194del , LRG_572t1:c.*191_*194del	NP_000304.2:n.*191_*194del
NM_001314077.1:c.*191_*194del , LRG_572t2:c.*191_*194del	NP_001301006.1:n.*191_*194del
NM_000313.4:c.*191_*194del MANE Select	NP_000304.2:n.*191_*194del
NM_001314077.2:c.*191_*194del	NP_001301006.1:n.*191_*194del