Canonical Allele Identifier: CA353674674

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646216T>A (hg19) ; chr3:g.93927372T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.112A>T	ENSP00000330021.7:p.Arg38Trp
ENST00000394236.9:c.112A>T MANE Select	ENSP00000377783.3:p.Arg38Trp
ENST00000407433.6:c.112A>T	ENSP00000385794.2:p.Arg38Trp
ENST00000472684.2:c.-282A>T	ENSP00000419616.2:n.-282A>T
ENST00000647936.1:c.112A>T	ENSP00000496822.1:p.Arg38Trp
ENST00000648381.1:n.280A>T
ENST00000648853.1:c.70A>T	ENSP00000497262.1:p.Arg24Trp
ENST00000649103.1:c.91A>T	ENSP00000497962.1:p.Arg31Trp
ENST00000650591.1:c.208A>T	ENSP00000497376.1:p.Arg70Trp
ENST00000348974.4:c.208A>T	ENSP00000330021.6:p.Arg70Trp
ENST00000394236.7:c.112A>T	ENSP00000377783.3:p.Arg38Trp
ENST00000407433.5:c.-282A>T	ENSP00000385794.1:n.-282A>T
ENST00000472684.1:c.-282A>T	ENSP00000419616.1:n.-282A>T
NM_000313.3:c.112A>T , LRG_572t1:c.112A>T	NP_000304.2:p.Arg38Trp
NM_001314077.1:c.208A>T , LRG_572t2:c.208A>T	NP_001301006.1:p.Arg70Trp
NM_000313.4:c.112A>T MANE Select	NP_000304.2:p.Arg38Trp
NM_001314077.2:c.208A>T	NP_001301006.1:p.Arg70Trp