Canonical Allele Identifier: CA353673462

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93624671A>T (hg19) ; chr3:g.93905827A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905827A>T , CM000665.2:g.93905827A>T	GRCh38
NC_000003.11:g.93624671A>T , CM000665.1:g.93624671A>T	GRCh37
NC_000003.10:g.95107361A>T	NCBI36
NG_009813.1:g.73264T>A , LRG_572:g.73264T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.558T>A	ENSP00000330021.7:p.Cys186Ter
ENST00000394236.9:c.558T>A MANE Select	ENSP00000377783.3:p.Cys186Ter
ENST00000407433.6:c.556+2T>A	ENSP00000385794.2:n.556+2T>A
ENST00000472684.2:c.165T>A	ENSP00000419616.2:p.Cys55Ter
ENST00000647936.1:c.558T>A	ENSP00000496822.1:p.Cys186Ter
ENST00000648381.1:n.726T>A
ENST00000648853.1:c.516T>A	ENSP00000497262.1:p.Cys172Ter
ENST00000649103.1:c.657T>A	ENSP00000497962.1:n.657T>A
ENST00000650591.1:c.654T>A	ENSP00000497376.1:p.Cys218Ter
ENST00000348974.4:c.654T>A	ENSP00000330021.6:p.Cys218Ter
ENST00000394236.7:c.558T>A	ENSP00000377783.3:p.Cys186Ter
ENST00000407433.5:c.165T>A	ENSP00000385794.1:p.Cys55Ter
ENST00000472684.1:c.165T>A	ENSP00000419616.1:p.Cys55Ter
NM_000313.3:c.558T>A , LRG_572t1:c.558T>A	NP_000304.2:p.Cys186Ter
NM_001314077.1:c.654T>A , LRG_572t2:c.654T>A	NP_001301006.1:p.Cys218Ter
NM_000313.4:c.558T>A MANE Select	NP_000304.2:p.Cys186Ter
NM_001314077.2:c.654T>A	NP_001301006.1:p.Cys218Ter