Canonical Allele Identifier: CA1385038271

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896541A= , CM000665.2:g.93896541A=	GRCh38
NC_000003.11:g.93615385A= , CM000665.1:g.93615385A=	GRCh37
NC_000003.10:g.95098075A=	NCBI36
NG_009813.1:g.82550T= , LRG_572:g.82550T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.965+35T=	ENSP00000330021.7:n.965+35T=
ENST00000394236.9:c.965+35T= MANE Select	ENSP00000377783.3:n.965+35T=
ENST00000407433.6:c.920+35T=	ENSP00000385794.2:n.920+35T=
ENST00000647936.1:c.965+35T=	ENSP00000496822.1:n.965+35T=
ENST00000648381.1:n.1133+35T=
ENST00000648853.1:c.923+35T=	ENSP00000497262.1:n.923+35T=
ENST00000649103.1:c.1064+35T=	ENSP00000497962.1:n.1064+35T=
ENST00000650591.1:c.1061+35T=	ENSP00000497376.1:n.1061+35T=
ENST00000394236.7:c.965+35T=	ENSP00000377783.3:n.965+35T=
ENST00000407433.5:c.572+35T=	ENSP00000385794.1:n.572+35T=
NM_000313.3:c.965+35T= , LRG_572t1:c.965+35T=	NP_000304.2:n.965+35T=
NM_001314077.1:c.1061+35T= , LRG_572t2:c.1061+35T=	NP_001301006.1:n.1061+35T=
NM_000313.4:c.965+35T= MANE Select	NP_000304.2:n.965+35T=
NM_001314077.2:c.1061+35T=	NP_001301006.1:n.1061+35T=