Canonical Allele Identifier: CA434460821

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615436A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896592A>G , CM000665.2:g.93896592A>G	GRCh38
NC_000003.11:g.93615436A>G , CM000665.1:g.93615436A>G	GRCh37
NC_000003.10:g.95098126A>G	NCBI36
NG_009813.1:g.82499T>C , LRG_572:g.82499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.949T>C	ENSP00000330021.7:p.Leu317=
ENST00000394236.9:c.949T>C MANE Select	ENSP00000377783.3:p.Leu317=
ENST00000407433.6:c.904T>C	ENSP00000385794.2:p.Leu302=
ENST00000647936.1:c.949T>C	ENSP00000496822.1:p.Leu317=
ENST00000648381.1:n.1117T>C
ENST00000648853.1:c.907T>C	ENSP00000497262.1:p.Leu303=
ENST00000649103.1:c.1048T>C	ENSP00000497962.1:n.1048T>C
ENST00000650591.1:c.1045T>C	ENSP00000497376.1:p.Leu349=
ENST00000394236.7:c.949T>C	ENSP00000377783.3:p.Leu317=
ENST00000407433.5:c.556T>C	ENSP00000385794.1:p.Leu186=
NM_000313.3:c.949T>C , LRG_572t1:c.949T>C	NP_000304.2:p.Leu317=
NM_001314077.1:c.1045T>C , LRG_572t2:c.1045T>C	NP_001301006.1:p.Leu349=
NM_000313.4:c.949T>C MANE Select	NP_000304.2:p.Leu317=
NM_001314077.2:c.1045T>C	NP_001301006.1:p.Leu349=