Canonical Allele Identifier: CA1385038347

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896703G= , CM000665.2:g.93896703G=	GRCh38
NC_000003.11:g.93615547G= , CM000665.1:g.93615547G=	GRCh37
NC_000003.10:g.95098237G=	NCBI36
NG_009813.1:g.82388C= , LRG_572:g.82388C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.850-12C=	ENSP00000330021.7:n.850-12C=
ENST00000394236.9:c.850-12C= MANE Select	ENSP00000377783.3:n.850-12C=
ENST00000407433.6:c.805-12C=	ENSP00000385794.2:n.805-12C=
ENST00000647936.1:c.850-12C=	ENSP00000496822.1:n.850-12C=
ENST00000648381.1:n.1018-12C=
ENST00000648853.1:c.808-12C=	ENSP00000497262.1:n.808-12C=
ENST00000649103.1:c.949-12C=	ENSP00000497962.1:n.949-12C=
ENST00000650591.1:c.946-12C=	ENSP00000497376.1:n.946-12C=
ENST00000394236.7:c.850-12C=	ENSP00000377783.3:n.850-12C=
ENST00000407433.5:c.457-12C=	ENSP00000385794.1:n.457-12C=
NM_000313.3:c.850-12C= , LRG_572t1:c.850-12C=	NP_000304.2:n.850-12C=
NM_001314077.1:c.946-12C= , LRG_572t2:c.946-12C=	NP_001301006.1:n.946-12C=
NM_000313.4:c.850-12C= MANE Select	NP_000304.2:n.850-12C=
NM_001314077.2:c.946-12C=	NP_001301006.1:n.946-12C=