Canonical Allele Identifier: CA353672774

Gene: PROS1

Linked Data

• gnomAD v4: 3-93898451-A-T
• MyVariant Identifiers: chr3:g.93617295A>T (hg19) ; chr3:g.93898451A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898451A>T , CM000665.2:g.93898451A>T	GRCh38
NC_000003.11:g.93617295A>T , CM000665.1:g.93617295A>T	GRCh37
NC_000003.10:g.95099985A>T	NCBI36
NG_009813.1:g.80640T>A , LRG_572:g.80640T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.846T>A	ENSP00000330021.7:p.Cys282Ter
ENST00000394236.9:c.846T>A MANE Select	ENSP00000377783.3:p.Cys282Ter
ENST00000407433.6:c.801T>A	ENSP00000385794.2:p.Cys267Ter
ENST00000647936.1:c.846T>A	ENSP00000496822.1:p.Cys282Ter
ENST00000648381.1:n.1014T>A
ENST00000648853.1:c.804T>A	ENSP00000497262.1:p.Cys268Ter
ENST00000649103.1:c.945T>A	ENSP00000497962.1:n.945T>A
ENST00000650591.1:c.942T>A	ENSP00000497376.1:p.Cys314Ter
ENST00000394236.7:c.846T>A	ENSP00000377783.3:p.Cys282Ter
ENST00000407433.5:c.453T>A	ENSP00000385794.1:p.Cys151Ter
NM_000313.3:c.846T>A , LRG_572t1:c.846T>A	NP_000304.2:p.Cys282Ter
NM_001314077.1:c.942T>A , LRG_572t2:c.942T>A	NP_001301006.1:p.Cys314Ter
NM_000313.4:c.846T>A MANE Select	NP_000304.2:p.Cys282Ter
NM_001314077.2:c.942T>A	NP_001301006.1:p.Cys314Ter