Canonical Allele Identifier: CA434463971

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93596009A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877165A>C , CM000665.2:g.93877165A>C	GRCh38
NC_000003.11:g.93596009A>C , CM000665.1:g.93596009A>C	GRCh37
NC_000003.10:g.95078699A>C	NCBI36
NG_009813.1:g.101926T>G , LRG_572:g.101926T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1671T>G	ENSP00000330021.7:p.Thr557=
ENST00000394236.9:c.1671T>G MANE Select	ENSP00000377783.3:p.Thr557=
ENST00000407433.6:c.1626T>G	ENSP00000385794.2:p.Thr542=
ENST00000647936.1:c.1644+1998T>G	ENSP00000496822.1:n.1644+1998T>G
ENST00000648381.1:n.1839T>G
ENST00000648853.1:c.1629T>G	ENSP00000497262.1:p.Thr543=
ENST00000649103.1:c.1770T>G	ENSP00000497962.1:n.1770T>G
ENST00000649585.1:c.614T>G	ENSP00000498163.1:n.614T>G
ENST00000650591.1:c.1767T>G	ENSP00000497376.1:p.Thr589=
ENST00000394236.7:c.1671T>G	ENSP00000377783.3:p.Thr557=
ENST00000407433.5:c.1278T>G	ENSP00000385794.1:p.Thr426=
NM_000313.3:c.1671T>G , LRG_572t1:c.1671T>G	NP_000304.2:p.Thr557=
NM_001314077.1:c.1767T>G , LRG_572t2:c.1767T>G	NP_001301006.1:p.Thr589=
NM_000313.4:c.1671T>G MANE Select	NP_000304.2:p.Thr557=
NM_001314077.2:c.1767T>G	NP_001301006.1:p.Thr589=