Canonical Allele Identifier: CA353673068

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619649T>G (hg19) ; chr3:g.93900805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900805T>G , CM000665.2:g.93900805T>G	GRCh38
NC_000003.11:g.93619649T>G , CM000665.1:g.93619649T>G	GRCh37
NC_000003.10:g.95102339T>G	NCBI36
NG_009813.1:g.78286A>C , LRG_572:g.78286A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.726A>C	ENSP00000330021.7:p.Glu242Asp
ENST00000394236.9:c.726A>C MANE Select	ENSP00000377783.3:p.Glu242Asp
ENST00000407433.6:c.681A>C	ENSP00000385794.2:p.Glu227Asp
ENST00000647936.1:c.726A>C	ENSP00000496822.1:p.Glu242Asp
ENST00000648381.1:n.894A>C
ENST00000648853.1:c.684A>C	ENSP00000497262.1:p.Glu228Asp
ENST00000649103.1:c.825A>C	ENSP00000497962.1:n.825A>C
ENST00000650591.1:c.822A>C	ENSP00000497376.1:p.Glu274Asp
ENST00000394236.7:c.726A>C	ENSP00000377783.3:p.Glu242Asp
ENST00000407433.5:c.333A>C	ENSP00000385794.1:p.Glu111Asp
NM_000313.3:c.726A>C , LRG_572t1:c.726A>C	NP_000304.2:p.Glu242Asp
NM_001314077.1:c.822A>C , LRG_572t2:c.822A>C	NP_001301006.1:p.Glu274Asp
NM_000313.4:c.726A>C MANE Select	NP_000304.2:p.Glu242Asp
NM_001314077.2:c.822A>C	NP_001301006.1:p.Glu274Asp