Canonical Allele Identifier: CA78505674

Gene: PROS1

Linked Data

• dbSNP Id: rs764911524
• MyVariant Identifiers: chr3:g.93646161C>T (hg19) ; chr3:g.93927317C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927317C>T , CM000665.2:g.93927317C>T	GRCh38
NC_000003.11:g.93646161C>T , CM000665.1:g.93646161C>T	GRCh37
NC_000003.10:g.95128851C>T	NCBI36
NG_009813.1:g.51774G>A , LRG_572:g.51774G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.167G>A	ENSP00000330021.7:p.Arg56Lys
ENST00000394236.9:c.167G>A MANE Select	ENSP00000377783.3:p.Arg56Lys
ENST00000407433.6:c.167G>A	ENSP00000385794.2:p.Arg56Lys
ENST00000472684.2:c.-227G>A	ENSP00000419616.2:n.-227G>A
ENST00000647936.1:c.167G>A	ENSP00000496822.1:p.Arg56Lys
ENST00000648381.1:n.335G>A
ENST00000648853.1:c.125G>A	ENSP00000497262.1:p.Arg42Lys
ENST00000649103.1:c.146G>A	ENSP00000497962.1:p.Arg49Lys
ENST00000650591.1:c.263G>A	ENSP00000497376.1:p.Arg88Lys
ENST00000348974.4:c.263G>A	ENSP00000330021.6:p.Arg88Lys
ENST00000394236.7:c.167G>A	ENSP00000377783.3:p.Arg56Lys
ENST00000407433.5:c.-227G>A	ENSP00000385794.1:n.-227G>A
ENST00000472684.1:c.-227G>A	ENSP00000419616.1:n.-227G>A
NM_000313.3:c.167G>A , LRG_572t1:c.167G>A	NP_000304.2:p.Arg56Lys
NM_001314077.1:c.263G>A , LRG_572t2:c.263G>A	NP_001301006.1:p.Arg88Lys
NM_000313.4:c.167G>A MANE Select	NP_000304.2:p.Arg56Lys
NM_001314077.2:c.263G>A	NP_001301006.1:p.Arg88Lys