Canonical Allele Identifier: CA434462765

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593090T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874246T>C , CM000665.2:g.93874246T>C	GRCh38
NC_000003.11:g.93593090T>C , CM000665.1:g.93593090T>C	GRCh37
NC_000003.10:g.95075780T>C	NCBI36
NG_009813.1:g.104845A>G , LRG_572:g.104845A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.2030A>G	ENSP00000330021.7:p.Ter677=
ENST00000394236.9:c.2030A>G MANE Select	ENSP00000377783.3:p.Ter677=
ENST00000407433.6:c.1985A>G	ENSP00000385794.2:p.Ter662=
ENST00000647936.1:c.*133A>G	ENSP00000496822.1:n.*133A>G
ENST00000648381.1:n.2198A>G
ENST00000648853.1:c.1988A>G	ENSP00000497262.1:p.Ter663=
ENST00000650591.1:c.2126A>G	ENSP00000497376.1:p.Ter709=
ENST00000394236.7:c.2030A>G	ENSP00000377783.3:p.Ter677=
ENST00000407433.5:c.1637A>G	ENSP00000385794.1:p.Ter546=
NM_000313.3:c.2030A>G , LRG_572t1:c.2030A>G	NP_000304.2:p.Ter677=
NM_001314077.1:c.2126A>G , LRG_572t2:c.2126A>G	NP_001301006.1:p.Ter709=
NM_000313.4:c.2030A>G MANE Select	NP_000304.2:p.Ter677=
NM_001314077.2:c.2126A>G	NP_001301006.1:p.Ter709=