Canonical Allele Identifier: CA434460823

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615437A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896593A>C , CM000665.2:g.93896593A>C	GRCh38
NC_000003.11:g.93615437A>C , CM000665.1:g.93615437A>C	GRCh37
NC_000003.10:g.95098127A>C	NCBI36
NG_009813.1:g.82498T>G , LRG_572:g.82498T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.948T>G	ENSP00000330021.7:p.Arg316=
ENST00000394236.9:c.948T>G MANE Select	ENSP00000377783.3:p.Arg316=
ENST00000407433.6:c.903T>G	ENSP00000385794.2:p.Arg301=
ENST00000647936.1:c.948T>G	ENSP00000496822.1:p.Arg316=
ENST00000648381.1:n.1116T>G
ENST00000648853.1:c.906T>G	ENSP00000497262.1:p.Arg302=
ENST00000649103.1:c.1047T>G	ENSP00000497962.1:n.1047T>G
ENST00000650591.1:c.1044T>G	ENSP00000497376.1:p.Arg348=
ENST00000394236.7:c.948T>G	ENSP00000377783.3:p.Arg316=
ENST00000407433.5:c.555T>G	ENSP00000385794.1:p.Arg185=
NM_000313.3:c.948T>G , LRG_572t1:c.948T>G	NP_000304.2:p.Arg316=
NM_001314077.1:c.1044T>G , LRG_572t2:c.1044T>G	NP_001301006.1:p.Arg348=
NM_000313.4:c.948T>G MANE Select	NP_000304.2:p.Arg316=
NM_001314077.2:c.1044T>G	NP_001301006.1:p.Arg348=