Canonical Allele Identifier: CA353672924

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93617360C>G (hg19) ; chr3:g.93898516C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898516C>G , CM000665.2:g.93898516C>G	GRCh38
NC_000003.11:g.93617360C>G , CM000665.1:g.93617360C>G	GRCh37
NC_000003.10:g.95100050C>G	NCBI36
NG_009813.1:g.80575G>C , LRG_572:g.80575G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.781G>C	ENSP00000330021.7:p.Gly261Arg
ENST00000394236.9:c.781G>C MANE Select	ENSP00000377783.3:p.Gly261Arg
ENST00000407433.6:c.736G>C	ENSP00000385794.2:p.Gly246Arg
ENST00000647936.1:c.781G>C	ENSP00000496822.1:p.Gly261Arg
ENST00000648381.1:n.949G>C
ENST00000648853.1:c.739G>C	ENSP00000497262.1:p.Gly247Arg
ENST00000649103.1:c.880G>C	ENSP00000497962.1:n.880G>C
ENST00000650591.1:c.877G>C	ENSP00000497376.1:p.Gly293Arg
ENST00000394236.7:c.781G>C	ENSP00000377783.3:p.Gly261Arg
ENST00000407433.5:c.388G>C	ENSP00000385794.1:p.Gly130Arg
NM_000313.3:c.781G>C , LRG_572t1:c.781G>C	NP_000304.2:p.Gly261Arg
NM_001314077.1:c.877G>C , LRG_572t2:c.877G>C	NP_001301006.1:p.Gly293Arg
NM_000313.4:c.781G>C MANE Select	NP_000304.2:p.Gly261Arg
NM_001314077.2:c.877G>C	NP_001301006.1:p.Gly293Arg