Canonical Allele Identifier: CA544750414

Gene: PROS1

Linked Data

• dbSNP Id: rs1487963016
• gnomAD v2: 3-93615556-TAAAC-T
• gnomAD v4: 3-93896712-TAAAC-T
• MyVariant Identifiers: chr3:g.93615557_93615560del (hg19) ; chr3:g.93896713_93896716del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896715_93896718del , CM000665.2:g.93896715_93896718del	GRCh38
NC_000003.11:g.93615559_93615562del , CM000665.1:g.93615559_93615562del	GRCh37
NC_000003.10:g.95098249_95098252del	NCBI36
NG_009813.1:g.82375_82378del , LRG_572:g.82375_82378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.850-25_850-22del	ENSP00000330021.7:n.850-25_850-22del
ENST00000394236.9:c.850-25_850-22del MANE Select	ENSP00000377783.3:n.850-25_850-22del
ENST00000407433.6:c.805-25_805-22del	ENSP00000385794.2:n.805-25_805-22del
ENST00000647936.1:c.850-25_850-22del	ENSP00000496822.1:n.850-25_850-22del
ENST00000648381.1:n.1018-25_1018-22del
ENST00000648853.1:c.808-25_808-22del	ENSP00000497262.1:n.808-25_808-22del
ENST00000649103.1:c.949-25_949-22del	ENSP00000497962.1:n.949-25_949-22del
ENST00000650591.1:c.946-25_946-22del	ENSP00000497376.1:n.946-25_946-22del
ENST00000394236.7:c.850-25_850-22del	ENSP00000377783.3:n.850-25_850-22del
ENST00000407433.5:c.457-25_457-22del	ENSP00000385794.1:n.457-25_457-22del
NM_000313.3:c.850-25_850-22del , LRG_572t1:c.850-25_850-22del	NP_000304.2:n.850-25_850-22del
NM_001314077.1:c.946-25_946-22del , LRG_572t2:c.946-25_946-22del	NP_001301006.1:n.946-25_946-22del
NM_000313.4:c.850-25_850-22del MANE Select	NP_000304.2:n.850-25_850-22del
NM_001314077.2:c.946-25_946-22del	NP_001301006.1:n.946-25_946-22del