Canonical Allele Identifier: CA1385026816

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874083C= , CM000665.2:g.93874083C=	GRCh38
NC_000003.11:g.93592927C= , CM000665.1:g.93592927C=	GRCh37
NC_000003.10:g.95075617C=	NCBI36
NG_009813.1:g.105008G= , LRG_572:g.105008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+161G=	ENSP00000330021.7:n.*1+161G=
ENST00000394236.9:c.*162G= MANE Select	ENSP00000377783.3:n.*162G=
ENST00000407433.6:c.*162G=	ENSP00000385794.2:n.*162G=
ENST00000647936.1:c.*296G=	ENSP00000496822.1:n.*296G=
ENST00000648381.1:n.2361G=
ENST00000648853.1:c.*162G=	ENSP00000497262.1:n.*162G=
ENST00000650591.1:c.*162G=	ENSP00000497376.1:n.*162G=
ENST00000394236.7:c.*162G=	ENSP00000377783.3:n.*162G=
ENST00000407433.5:c.*162G=	ENSP00000385794.1:n.*162G=
NM_000313.3:c.*162G= , LRG_572t1:c.*162G=	NP_000304.2:n.*162G=
NM_001314077.1:c.*162G= , LRG_572t2:c.*162G=	NP_001301006.1:n.*162G=
NM_000313.4:c.*162G= MANE Select	NP_000304.2:n.*162G=
NM_001314077.2:c.*162G=	NP_001301006.1:n.*162G=