Canonical Allele Identifier: CA434459784

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611882G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893038G>T , CM000665.2:g.93893038G>T	GRCh38
NC_000003.11:g.93611882G>T , CM000665.1:g.93611882G>T	GRCh37
NC_000003.10:g.95094572G>T	NCBI36
NG_009813.1:g.86053C>A , LRG_572:g.86053C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1050C>A	ENSP00000330021.7:p.Leu350=
ENST00000394236.9:c.1050C>A MANE Select	ENSP00000377783.3:p.Leu350=
ENST00000407433.6:c.1005C>A	ENSP00000385794.2:p.Leu335=
ENST00000647936.1:c.1050C>A	ENSP00000496822.1:p.Leu350=
ENST00000648381.1:n.1218C>A
ENST00000648853.1:c.1008C>A	ENSP00000497262.1:p.Leu336=
ENST00000649103.1:c.1149C>A	ENSP00000497962.1:n.1149C>A
ENST00000650591.1:c.1146C>A	ENSP00000497376.1:p.Leu382=
ENST00000394236.7:c.1050C>A	ENSP00000377783.3:p.Leu350=
ENST00000407433.5:c.657C>A	ENSP00000385794.1:p.Leu219=
NM_000313.3:c.1050C>A , LRG_572t1:c.1050C>A	NP_000304.2:p.Leu350=
NM_001314077.1:c.1146C>A , LRG_572t2:c.1146C>A	NP_001301006.1:p.Leu382=
NM_000313.4:c.1050C>A MANE Select	NP_000304.2:p.Leu350=
NM_001314077.2:c.1146C>A	NP_001301006.1:p.Leu382=