Canonical Allele Identifier: CA1385026663

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873790C= , CM000665.2:g.93873790C=	GRCh38
NC_000003.11:g.93592634C= , CM000665.1:g.93592634C=	GRCh37
NC_000003.10:g.95075324C=	NCBI36
NG_009813.1:g.105301G= , LRG_572:g.105301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-377G=	ENSP00000330021.7:n.*2-377G=
ENST00000394236.9:c.*455G= MANE Select	ENSP00000377783.3:n.*455G=
ENST00000407433.6:c.*455G=	ENSP00000385794.2:n.*455G=
ENST00000647936.1:c.*589G=	ENSP00000496822.1:n.*589G=
ENST00000648381.1:n.2654G=
ENST00000648853.1:c.*455G=	ENSP00000497262.1:n.*455G=
ENST00000650591.1:c.*455G=	ENSP00000497376.1:n.*455G=
ENST00000394236.7:c.*455G=	ENSP00000377783.3:n.*455G=
ENST00000407433.5:c.*455G=	ENSP00000385794.1:n.*455G=
NM_000313.3:c.*455G= , LRG_572t1:c.*455G=	NP_000304.2:n.*455G=
NM_001314077.1:c.*455G= , LRG_572t2:c.*455G=	NP_001301006.1:n.*455G=
NM_000313.4:c.*455G= MANE Select	NP_000304.2:n.*455G=
NM_001314077.2:c.*455G=	NP_001301006.1:n.*455G=