Canonical Allele Identifier: CA353672608

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615469A>T (hg19) ; chr3:g.93896625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896625A>T , CM000665.2:g.93896625A>T	GRCh38
NC_000003.11:g.93615469A>T , CM000665.1:g.93615469A>T	GRCh37
NC_000003.10:g.95098159A>T	NCBI36
NG_009813.1:g.82466T>A , LRG_572:g.82466T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.916T>A	ENSP00000330021.7:p.Phe306Ile
ENST00000394236.9:c.916T>A MANE Select	ENSP00000377783.3:p.Phe306Ile
ENST00000407433.6:c.871T>A	ENSP00000385794.2:p.Phe291Ile
ENST00000647936.1:c.916T>A	ENSP00000496822.1:p.Phe306Ile
ENST00000648381.1:n.1084T>A
ENST00000648853.1:c.874T>A	ENSP00000497262.1:p.Phe292Ile
ENST00000649103.1:c.1015T>A	ENSP00000497962.1:n.1015T>A
ENST00000650591.1:c.1012T>A	ENSP00000497376.1:p.Phe338Ile
ENST00000394236.7:c.916T>A	ENSP00000377783.3:p.Phe306Ile
ENST00000407433.5:c.523T>A	ENSP00000385794.1:p.Phe175Ile
NM_000313.3:c.916T>A , LRG_572t1:c.916T>A	NP_000304.2:p.Phe306Ile
NM_001314077.1:c.1012T>A , LRG_572t2:c.1012T>A	NP_001301006.1:p.Phe338Ile
NM_000313.4:c.916T>A MANE Select	NP_000304.2:p.Phe306Ile
NM_001314077.2:c.1012T>A	NP_001301006.1:p.Phe338Ile