Canonical Allele Identifier: CA353673483

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93624681T>G (hg19) ; chr3:g.93905837T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905837T>G , CM000665.2:g.93905837T>G	GRCh38
NC_000003.11:g.93624681T>G , CM000665.1:g.93624681T>G	GRCh37
NC_000003.10:g.95107371T>G	NCBI36
NG_009813.1:g.73254A>C , LRG_572:g.73254A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.548A>C	ENSP00000330021.7:p.His183Pro
ENST00000394236.9:c.548A>C MANE Select	ENSP00000377783.3:p.His183Pro
ENST00000407433.6:c.548A>C	ENSP00000385794.2:p.His183Pro
ENST00000472684.2:c.155A>C	ENSP00000419616.2:p.His52Pro
ENST00000647936.1:c.548A>C	ENSP00000496822.1:p.His183Pro
ENST00000648381.1:n.716A>C
ENST00000648853.1:c.506A>C	ENSP00000497262.1:p.His169Pro
ENST00000649103.1:c.647A>C	ENSP00000497962.1:n.647A>C
ENST00000650591.1:c.644A>C	ENSP00000497376.1:p.His215Pro
ENST00000348974.4:c.644A>C	ENSP00000330021.6:p.His215Pro
ENST00000394236.7:c.548A>C	ENSP00000377783.3:p.His183Pro
ENST00000407433.5:c.155A>C	ENSP00000385794.1:p.His52Pro
ENST00000472684.1:c.155A>C	ENSP00000419616.1:p.His52Pro
NM_000313.3:c.548A>C , LRG_572t1:c.548A>C	NP_000304.2:p.His183Pro
NM_001314077.1:c.644A>C , LRG_572t2:c.644A>C	NP_001301006.1:p.His215Pro
NM_000313.4:c.548A>C MANE Select	NP_000304.2:p.His183Pro
NM_001314077.2:c.644A>C	NP_001301006.1:p.His215Pro