Canonical Allele Identifier: CA1385039141

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898562A= , CM000665.2:g.93898562A=	GRCh38
NC_000003.11:g.93617406A= , CM000665.1:g.93617406A=	GRCh37
NC_000003.10:g.95100096A=	NCBI36
NG_009813.1:g.80529T= , LRG_572:g.80529T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.735T=	ENSP00000330021.7:p.Asp245=
ENST00000394236.9:c.735T= MANE Select	ENSP00000377783.3:p.Asp245=
ENST00000407433.6:c.690T=	ENSP00000385794.2:p.Asp230=
ENST00000647936.1:c.735T=	ENSP00000496822.1:p.Asp245=
ENST00000648381.1:n.903T=
ENST00000648853.1:c.693T=	ENSP00000497262.1:p.Asp231=
ENST00000649103.1:c.834T=	ENSP00000497962.1:n.834T=
ENST00000650591.1:c.831T=	ENSP00000497376.1:p.Asp277=
ENST00000394236.7:c.735T=	ENSP00000377783.3:p.Asp245=
ENST00000407433.5:c.342T=	ENSP00000385794.1:p.Asp114=
NM_000313.3:c.735T= , LRG_572t1:c.735T=	NP_000304.2:p.Asp245=
NM_001314077.1:c.831T= , LRG_572t2:c.831T=	NP_001301006.1:p.Asp277=
NM_000313.4:c.735T= MANE Select	NP_000304.2:p.Asp245=
NM_001314077.2:c.831T=	NP_001301006.1:p.Asp277=