Canonical Allele Identifier: CA353673406

Gene: PROS1

Linked Data

• gnomAD v4: 3-93905802-T-C
• MyVariant Identifiers: chr3:g.93624646T>C (hg19) ; chr3:g.93905802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905802T>C , CM000665.2:g.93905802T>C	GRCh38
NC_000003.11:g.93624646T>C , CM000665.1:g.93624646T>C	GRCh37
NC_000003.10:g.95107336T>C	NCBI36
NG_009813.1:g.73289A>G , LRG_572:g.73289A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.583A>G	ENSP00000330021.7:p.Asn195Asp
ENST00000394236.9:c.583A>G MANE Select	ENSP00000377783.3:p.Asn195Asp
ENST00000407433.6:c.556+27A>G	ENSP00000385794.2:n.556+27A>G
ENST00000647936.1:c.583A>G	ENSP00000496822.1:p.Asn195Asp
ENST00000648381.1:n.751A>G
ENST00000648853.1:c.541A>G	ENSP00000497262.1:p.Asn181Asp
ENST00000649103.1:c.682A>G	ENSP00000497962.1:n.682A>G
ENST00000650591.1:c.679A>G	ENSP00000497376.1:p.Asn227Asp
ENST00000348974.4:c.679A>G	ENSP00000330021.6:p.Asn227Asp
ENST00000394236.7:c.583A>G	ENSP00000377783.3:p.Asn195Asp
ENST00000407433.5:c.190A>G	ENSP00000385794.1:p.Asn64Asp
NM_000313.3:c.583A>G , LRG_572t1:c.583A>G	NP_000304.2:p.Asn195Asp
NM_001314077.1:c.679A>G , LRG_572t2:c.679A>G	NP_001301006.1:p.Asn227Asp
NM_000313.4:c.583A>G MANE Select	NP_000304.2:p.Asn195Asp
NM_001314077.2:c.679A>G	NP_001301006.1:p.Asn227Asp