Canonical Allele Identifier: CA353672720

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615519A>C (hg19) ; chr3:g.93896675A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896675A>C , CM000665.2:g.93896675A>C	GRCh38
NC_000003.11:g.93615519A>C , CM000665.1:g.93615519A>C	GRCh37
NC_000003.10:g.95098209A>C	NCBI36
NG_009813.1:g.82416T>G , LRG_572:g.82416T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.866T>G	ENSP00000330021.7:p.Leu289Arg
ENST00000394236.9:c.866T>G MANE Select	ENSP00000377783.3:p.Leu289Arg
ENST00000407433.6:c.821T>G	ENSP00000385794.2:p.Leu274Arg
ENST00000647936.1:c.866T>G	ENSP00000496822.1:p.Leu289Arg
ENST00000648381.1:n.1034T>G
ENST00000648853.1:c.824T>G	ENSP00000497262.1:p.Leu275Arg
ENST00000649103.1:c.965T>G	ENSP00000497962.1:n.965T>G
ENST00000650591.1:c.962T>G	ENSP00000497376.1:p.Leu321Arg
ENST00000394236.7:c.866T>G	ENSP00000377783.3:p.Leu289Arg
ENST00000407433.5:c.473T>G	ENSP00000385794.1:p.Leu158Arg
NM_000313.3:c.866T>G , LRG_572t1:c.866T>G	NP_000304.2:p.Leu289Arg
NM_001314077.1:c.962T>G , LRG_572t2:c.962T>G	NP_001301006.1:p.Leu321Arg
NM_000313.4:c.866T>G MANE Select	NP_000304.2:p.Leu289Arg
NM_001314077.2:c.962T>G	NP_001301006.1:p.Leu321Arg