Canonical Allele Identifier: CA1385036816

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893002C= , CM000665.2:g.93893002C=	GRCh38
NC_000003.11:g.93611846C= , CM000665.1:g.93611846C=	GRCh37
NC_000003.10:g.95094536C=	NCBI36
NG_009813.1:g.86089G= , LRG_572:g.86089G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1086G=	ENSP00000330021.7:p.Gln362=
ENST00000394236.9:c.1086G= MANE Select	ENSP00000377783.3:p.Gln362=
ENST00000407433.6:c.1041G=	ENSP00000385794.2:p.Gln347=
ENST00000647936.1:c.1086G=	ENSP00000496822.1:p.Gln362=
ENST00000648381.1:n.1254G=
ENST00000648853.1:c.1044G=	ENSP00000497262.1:p.Gln348=
ENST00000649103.1:c.1185G=	ENSP00000497962.1:n.1185G=
ENST00000650591.1:c.1182G=	ENSP00000497376.1:p.Gln394=
ENST00000394236.7:c.1086G=	ENSP00000377783.3:p.Gln362=
ENST00000407433.5:c.693G=	ENSP00000385794.1:p.Gln231=
NM_000313.3:c.1086G= , LRG_572t1:c.1086G=	NP_000304.2:p.Gln362=
NM_001314077.1:c.1182G= , LRG_572t2:c.1182G=	NP_001301006.1:p.Gln394=
NM_000313.4:c.1086G= MANE Select	NP_000304.2:p.Gln362=
NM_001314077.2:c.1182G=	NP_001301006.1:p.Gln394=