Canonical Allele Identifier: CA434464458

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598112A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879268A>G , CM000665.2:g.93879268A>G	GRCh38
NC_000003.11:g.93598112A>G , CM000665.1:g.93598112A>G	GRCh37
NC_000003.10:g.95080802A>G	NCBI36
NG_009813.1:g.99823T>C , LRG_572:g.99823T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1539T>C	ENSP00000330021.7:p.Asn513=
ENST00000394236.9:c.1539T>C MANE Select	ENSP00000377783.3:p.Asn513=
ENST00000407433.6:c.1494T>C	ENSP00000385794.2:p.Asn498=
ENST00000647936.1:c.1539T>C	ENSP00000496822.1:p.Asn513=
ENST00000648381.1:n.1707T>C
ENST00000648853.1:c.1497T>C	ENSP00000497262.1:p.Asn499=
ENST00000649103.1:c.1638T>C	ENSP00000497962.1:n.1638T>C
ENST00000649585.1:c.482T>C	ENSP00000498163.1:n.482T>C
ENST00000650591.1:c.1635T>C	ENSP00000497376.1:p.Asn545=
ENST00000394236.7:c.1539T>C	ENSP00000377783.3:p.Asn513=
ENST00000407433.5:c.1146T>C	ENSP00000385794.1:p.Asn382=
NM_000313.3:c.1539T>C , LRG_572t1:c.1539T>C	NP_000304.2:p.Asn513=
NM_001314077.1:c.1635T>C , LRG_572t2:c.1635T>C	NP_001301006.1:p.Asn545=
NM_000313.4:c.1539T>C MANE Select	NP_000304.2:p.Asn513=
NM_001314077.2:c.1635T>C	NP_001301006.1:p.Asn545=