Canonical Allele Identifier: CA353668910

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93884869G>C , CM000665.2:g.93884869G>C	GRCh38
NC_000003.11:g.93603713G>C , CM000665.1:g.93603713G>C	GRCh37
NC_000003.10:g.95086403G>C	NCBI36
NG_009813.1:g.94222C>G , LRG_572:g.94222C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.1351C>G MANE Select	NP_000304.2:p.Arg451Gly
ENST00000394236.9:c.1351C>G MANE Select	ENSP00000377783.3:p.Arg451Gly
NM_000313.3:c.1351C>G , LRG_572t1:c.1351C>G	NP_000304.2:p.Arg451Gly
NM_001314077.1:c.1447C>G , LRG_572t2:c.1447C>G	NP_001301006.1:p.Arg483Gly
NM_001314077.2:c.1447C>G	NP_001301006.1:p.Arg483Gly
ENST00000348974.5:c.1351C>G	ENSP00000330021.7:p.Arg451Gly
ENST00000394236.7:c.1351C>G	ENSP00000377783.3:p.Arg451Gly
ENST00000407433.5:c.958C>G	ENSP00000385794.1:p.Arg320Gly
ENST00000407433.6:c.1306C>G	ENSP00000385794.2:p.Arg436Gly
ENST00000647936.1:c.1351C>G	ENSP00000496822.1:p.Arg451Gly
ENST00000648381.1:n.1519C>G
ENST00000648853.1:c.1309C>G	ENSP00000497262.1:p.Arg437Gly
ENST00000649103.1:c.1450C>G	ENSP00000497962.1:n.1450C>G
ENST00000649585.1:c.106C>G	ENSP00000498163.1:p.Arg36Gly
ENST00000650591.1:c.1447C>G	ENSP00000497376.1:p.Arg483Gly