Canonical Allele Identifier: CA353672724

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615520G>T (hg19) ; chr3:g.93896676G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896676G>T , CM000665.2:g.93896676G>T	GRCh38
NC_000003.11:g.93615520G>T , CM000665.1:g.93615520G>T	GRCh37
NC_000003.10:g.95098210G>T	NCBI36
NG_009813.1:g.82415C>A , LRG_572:g.82415C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.865C>A	ENSP00000330021.7:p.Leu289Ile
ENST00000394236.9:c.865C>A MANE Select	ENSP00000377783.3:p.Leu289Ile
ENST00000407433.6:c.820C>A	ENSP00000385794.2:p.Leu274Ile
ENST00000647936.1:c.865C>A	ENSP00000496822.1:p.Leu289Ile
ENST00000648381.1:n.1033C>A
ENST00000648853.1:c.823C>A	ENSP00000497262.1:p.Leu275Ile
ENST00000649103.1:c.964C>A	ENSP00000497962.1:n.964C>A
ENST00000650591.1:c.961C>A	ENSP00000497376.1:p.Leu321Ile
ENST00000394236.7:c.865C>A	ENSP00000377783.3:p.Leu289Ile
ENST00000407433.5:c.472C>A	ENSP00000385794.1:p.Leu158Ile
NM_000313.3:c.865C>A , LRG_572t1:c.865C>A	NP_000304.2:p.Leu289Ile
NM_001314077.1:c.961C>A , LRG_572t2:c.961C>A	NP_001301006.1:p.Leu321Ile
NM_000313.4:c.865C>A MANE Select	NP_000304.2:p.Leu289Ile
NM_001314077.2:c.961C>A	NP_001301006.1:p.Leu321Ile