Canonical Allele Identifier: CA353672726

Gene: PROS1

Linked Data

• ClinVar Variation Id: 1456211
• ClinVar RCV Id: RCV001951037
• dbSNP Id: rs554787241
• MyVariant Identifiers: chr3:g.93615521G>T (hg19) ; chr3:g.93896677G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896677G>T , CM000665.2:g.93896677G>T	GRCh38
NC_000003.11:g.93615521G>T , CM000665.1:g.93615521G>T	GRCh37
NC_000003.10:g.95098211G>T	NCBI36
NG_009813.1:g.82414C>A , LRG_572:g.82414C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.864C>A	ENSP00000330021.7:p.Cys288Ter
ENST00000394236.9:c.864C>A MANE Select	ENSP00000377783.3:p.Cys288Ter
ENST00000407433.6:c.819C>A	ENSP00000385794.2:p.Cys273Ter
ENST00000647936.1:c.864C>A	ENSP00000496822.1:p.Cys288Ter
ENST00000648381.1:n.1032C>A
ENST00000648853.1:c.822C>A	ENSP00000497262.1:p.Cys274Ter
ENST00000649103.1:c.963C>A	ENSP00000497962.1:n.963C>A
ENST00000650591.1:c.960C>A	ENSP00000497376.1:p.Cys320Ter
ENST00000394236.7:c.864C>A	ENSP00000377783.3:p.Cys288Ter
ENST00000407433.5:c.471C>A	ENSP00000385794.1:p.Cys157Ter
NM_000313.3:c.864C>A , LRG_572t1:c.864C>A	NP_000304.2:p.Cys288Ter
NM_001314077.1:c.960C>A , LRG_572t2:c.960C>A	NP_001301006.1:p.Cys320Ter
NM_000313.4:c.864C>A MANE Select	NP_000304.2:p.Cys288Ter
NM_001314077.2:c.960C>A	NP_001301006.1:p.Cys320Ter