Canonical Allele Identifier: CA353672719

Gene: PROS1

Linked Data

• COSMIC: COSM3916744
• MyVariant Identifiers: chr3:g.93615517G>A (hg19) ; chr3:g.93896673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896673G>A , CM000665.2:g.93896673G>A	GRCh38
NC_000003.11:g.93615517G>A , CM000665.1:g.93615517G>A	GRCh37
NC_000003.10:g.95098207G>A	NCBI36
NG_009813.1:g.82418C>T , LRG_572:g.82418C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.868C>T	ENSP00000330021.7:p.Pro290Ser
ENST00000394236.9:c.868C>T MANE Select	ENSP00000377783.3:p.Pro290Ser
ENST00000407433.6:c.823C>T	ENSP00000385794.2:p.Pro275Ser
ENST00000647936.1:c.868C>T	ENSP00000496822.1:p.Pro290Ser
ENST00000648381.1:n.1036C>T
ENST00000648853.1:c.826C>T	ENSP00000497262.1:p.Pro276Ser
ENST00000649103.1:c.967C>T	ENSP00000497962.1:n.967C>T
ENST00000650591.1:c.964C>T	ENSP00000497376.1:p.Pro322Ser
ENST00000394236.7:c.868C>T	ENSP00000377783.3:p.Pro290Ser
ENST00000407433.5:c.475C>T	ENSP00000385794.1:p.Pro159Ser
NM_000313.3:c.868C>T , LRG_572t1:c.868C>T	NP_000304.2:p.Pro290Ser
NM_001314077.1:c.964C>T , LRG_572t2:c.964C>T	NP_001301006.1:p.Pro322Ser
NM_000313.4:c.868C>T MANE Select	NP_000304.2:p.Pro290Ser
NM_001314077.2:c.964C>T	NP_001301006.1:p.Pro322Ser