Canonical Allele Identifier: CA434462911

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646216T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927372T>G , CM000665.2:g.93927372T>G	GRCh38
NC_000003.11:g.93646216T>G , CM000665.1:g.93646216T>G	GRCh37
NC_000003.10:g.95128906T>G	NCBI36
NG_009813.1:g.51719A>C , LRG_572:g.51719A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.112A>C	ENSP00000330021.7:p.Arg38=
ENST00000394236.9:c.112A>C MANE Select	ENSP00000377783.3:p.Arg38=
ENST00000407433.6:c.112A>C	ENSP00000385794.2:p.Arg38=
ENST00000472684.2:c.-282A>C	ENSP00000419616.2:n.-282A>C
ENST00000647936.1:c.112A>C	ENSP00000496822.1:p.Arg38=
ENST00000648381.1:n.280A>C
ENST00000648853.1:c.70A>C	ENSP00000497262.1:p.Arg24=
ENST00000649103.1:c.91A>C	ENSP00000497962.1:p.Arg31=
ENST00000650591.1:c.208A>C	ENSP00000497376.1:p.Arg70=
ENST00000348974.4:c.208A>C	ENSP00000330021.6:p.Arg70=
ENST00000394236.7:c.112A>C	ENSP00000377783.3:p.Arg38=
ENST00000407433.5:c.-282A>C	ENSP00000385794.1:n.-282A>C
ENST00000472684.1:c.-282A>C	ENSP00000419616.1:n.-282A>C
NM_000313.3:c.112A>C , LRG_572t1:c.112A>C	NP_000304.2:p.Arg38=
NM_001314077.1:c.208A>C , LRG_572t2:c.208A>C	NP_001301006.1:p.Arg70=
NM_000313.4:c.112A>C MANE Select	NP_000304.2:p.Arg38=
NM_001314077.2:c.208A>C	NP_001301006.1:p.Arg70=