Canonical Allele Identifier: CA1385026928

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874328C= , CM000665.2:g.93874328C=	GRCh38
NC_000003.11:g.93593172C= , CM000665.1:g.93593172C=	GRCh37
NC_000003.10:g.95075862C=	NCBI36
NG_009813.1:g.104763G= , LRG_572:g.104763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1948G=	ENSP00000330021.7:p.Asp650=
ENST00000394236.9:c.1948G= MANE Select	ENSP00000377783.3:p.Asp650=
ENST00000407433.6:c.1903G=	ENSP00000385794.2:p.Asp635=
ENST00000647936.1:c.*51G=	ENSP00000496822.1:n.*51G=
ENST00000648381.1:n.2116G=
ENST00000648853.1:c.1906G=	ENSP00000497262.1:p.Asp636=
ENST00000650591.1:c.2044G=	ENSP00000497376.1:p.Asp682=
ENST00000394236.7:c.1948G=	ENSP00000377783.3:p.Asp650=
ENST00000407433.5:c.1555G=	ENSP00000385794.1:p.Asp519=
NM_000313.3:c.1948G= , LRG_572t1:c.1948G=	NP_000304.2:p.Asp650=
NM_001314077.1:c.2044G= , LRG_572t2:c.2044G=	NP_001301006.1:p.Asp682=
NM_000313.4:c.1948G= MANE Select	NP_000304.2:p.Asp650=
NM_001314077.2:c.2044G=	NP_001301006.1:p.Asp682=