Canonical Allele Identifier: CA1385038299

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896595G= , CM000665.2:g.93896595G=	GRCh38
NC_000003.11:g.93615439G= , CM000665.1:g.93615439G=	GRCh37
NC_000003.10:g.95098129G=	NCBI36
NG_009813.1:g.82496C= , LRG_572:g.82496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.946C=	ENSP00000330021.7:p.Arg316=
ENST00000394236.9:c.946C= MANE Select	ENSP00000377783.3:p.Arg316=
ENST00000407433.6:c.901C=	ENSP00000385794.2:p.Arg301=
ENST00000647936.1:c.946C=	ENSP00000496822.1:p.Arg316=
ENST00000648381.1:n.1114C=
ENST00000648853.1:c.904C=	ENSP00000497262.1:p.Arg302=
ENST00000649103.1:c.1045C=	ENSP00000497962.1:n.1045C=
ENST00000650591.1:c.1042C=	ENSP00000497376.1:p.Arg348=
ENST00000394236.7:c.946C=	ENSP00000377783.3:p.Arg316=
ENST00000407433.5:c.553C=	ENSP00000385794.1:p.Arg185=
NM_000313.3:c.946C= , LRG_572t1:c.946C=	NP_000304.2:p.Arg316=
NM_001314077.1:c.1042C= , LRG_572t2:c.1042C=	NP_001301006.1:p.Arg348=
NM_000313.4:c.946C= MANE Select	NP_000304.2:p.Arg316=
NM_001314077.2:c.1042C=	NP_001301006.1:p.Arg348=