Canonical Allele Identifier: CA353672733

Gene: PROS1

Linked Data

• dbSNP Id: rs753269101
• gnomAD v4: 3-93896681-A-C
• MyVariant Identifiers: chr3:g.93615525A>C (hg19) ; chr3:g.93896681A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896681A>C , CM000665.2:g.93896681A>C	GRCh38
NC_000003.11:g.93615525A>C , CM000665.1:g.93615525A>C	GRCh37
NC_000003.10:g.95098215A>C	NCBI36
NG_009813.1:g.82410T>G , LRG_572:g.82410T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.860T>G	ENSP00000330021.7:p.Val287Gly
ENST00000394236.9:c.860T>G MANE Select	ENSP00000377783.3:p.Val287Gly
ENST00000407433.6:c.815T>G	ENSP00000385794.2:p.Val272Gly
ENST00000647936.1:c.860T>G	ENSP00000496822.1:p.Val287Gly
ENST00000648381.1:n.1028T>G
ENST00000648853.1:c.818T>G	ENSP00000497262.1:p.Val273Gly
ENST00000649103.1:c.959T>G	ENSP00000497962.1:n.959T>G
ENST00000650591.1:c.956T>G	ENSP00000497376.1:p.Val319Gly
ENST00000394236.7:c.860T>G	ENSP00000377783.3:p.Val287Gly
ENST00000407433.5:c.467T>G	ENSP00000385794.1:p.Val156Gly
NM_000313.3:c.860T>G , LRG_572t1:c.860T>G	NP_000304.2:p.Val287Gly
NM_001314077.1:c.956T>G , LRG_572t2:c.956T>G	NP_001301006.1:p.Val319Gly
NM_000313.4:c.860T>G MANE Select	NP_000304.2:p.Val287Gly
NM_001314077.2:c.956T>G	NP_001301006.1:p.Val319Gly