Canonical Allele Identifier: CA912683035

Gene: PROS1

Linked Data

• dbSNP Id: rs1282076870
• gnomAD v4: 3-93873835-CA-C
• MyVariant Identifiers: chr3:g.93592680del (hg19) ; chr3:g.93873836del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873839del , CM000665.2:g.93873839del	GRCh38
NC_000003.11:g.93592683del , CM000665.1:g.93592683del	GRCh37
NC_000003.10:g.95075373del	NCBI36
NG_009813.1:g.105255del , LRG_572:g.105255del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+408del	ENSP00000330021.7:n.*1+408del
ENST00000394236.9:c.*409del MANE Select	ENSP00000377783.3:n.*409del
ENST00000407433.6:c.*409del	ENSP00000385794.2:n.*409del
ENST00000647936.1:c.*543del	ENSP00000496822.1:n.*543del
ENST00000648381.1:n.2608del
ENST00000648853.1:c.*409del	ENSP00000497262.1:n.*409del
ENST00000650591.1:c.*409del	ENSP00000497376.1:n.*409del
ENST00000394236.7:c.*409del	ENSP00000377783.3:n.*409del
ENST00000407433.5:c.*409del	ENSP00000385794.1:n.*409del
NM_000313.3:c.*409del , LRG_572t1:c.*409del	NP_000304.2:n.*409del
NM_001314077.1:c.*409del , LRG_572t2:c.*409del	NP_001301006.1:n.*409del
NM_000313.4:c.*409del MANE Select	NP_000304.2:n.*409del
NM_001314077.2:c.*409del	NP_001301006.1:n.*409del