Canonical Allele Identifier: CA1385038308

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896612A= , CM000665.2:g.93896612A=	GRCh38
NC_000003.11:g.93615456A= , CM000665.1:g.93615456A=	GRCh37
NC_000003.10:g.95098146A=	NCBI36
NG_009813.1:g.82479T= , LRG_572:g.82479T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.929T=	ENSP00000330021.7:p.Val310=
ENST00000394236.9:c.929T= MANE Select	ENSP00000377783.3:p.Val310=
ENST00000407433.6:c.884T=	ENSP00000385794.2:p.Val295=
ENST00000647936.1:c.929T=	ENSP00000496822.1:p.Val310=
ENST00000648381.1:n.1097T=
ENST00000648853.1:c.887T=	ENSP00000497262.1:p.Val296=
ENST00000649103.1:c.1028T=	ENSP00000497962.1:n.1028T=
ENST00000650591.1:c.1025T=	ENSP00000497376.1:p.Val342=
ENST00000394236.7:c.929T=	ENSP00000377783.3:p.Val310=
ENST00000407433.5:c.536T=	ENSP00000385794.1:p.Val179=
NM_000313.3:c.929T= , LRG_572t1:c.929T=	NP_000304.2:p.Val310=
NM_001314077.1:c.1025T= , LRG_572t2:c.1025T=	NP_001301006.1:p.Val342=
NM_000313.4:c.929T= MANE Select	NP_000304.2:p.Val310=
NM_001314077.2:c.1025T=	NP_001301006.1:p.Val342=