Canonical Allele Identifier: CA353673043
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93898566A>C , CM000665.2:g.93898566A>C GRCh38
NC_000003.11:g.93617410A>C , CM000665.1:g.93617410A>C GRCh37
NC_000003.10:g.95100100A>C NCBI36
NG_009813.1:g.80525T>G , LRG_572:g.80525T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.731T>G ENSP00000330021.7:p.Ile244Arg
ENST00000394236.9:c.731T>G MANE Select ENSP00000377783.3:p.Ile244Arg
ENST00000407433.6:c.686T>G ENSP00000385794.2:p.Ile229Arg
ENST00000647936.1:c.731T>G ENSP00000496822.1:p.Ile244Arg
ENST00000648381.1:n.899T>G
ENST00000648853.1:c.689T>G ENSP00000497262.1:p.Ile230Arg
ENST00000649103.1:c.830T>G ENSP00000497962.1:n.830T>G
ENST00000650591.1:c.827T>G ENSP00000497376.1:p.Ile276Arg
ENST00000394236.7:c.731T>G ENSP00000377783.3:p.Ile244Arg
ENST00000407433.5:c.338T>G ENSP00000385794.1:p.Ile113Arg
NM_000313.3:c.731T>G , LRG_572t1:c.731T>G NP_000304.2:p.Ile244Arg
NM_001314077.1:c.827T>G , LRG_572t2:c.827T>G NP_001301006.1:p.Ile276Arg
NM_000313.4:c.731T>G MANE Select NP_000304.2:p.Ile244Arg
NM_001314077.2:c.827T>G NP_001301006.1:p.Ile276Arg