Canonical Allele Identifier: CA1385026634

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873760G= , CM000665.2:g.93873760G=	GRCh38
NC_000003.11:g.93592604G= , CM000665.1:g.93592604G=	GRCh37
NC_000003.10:g.95075294G=	NCBI36
NG_009813.1:g.105331C= , LRG_572:g.105331C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-347C=	ENSP00000330021.7:n.*2-347C=
ENST00000394236.9:c.*485C= MANE Select	ENSP00000377783.3:n.*485C=
ENST00000407433.6:c.*485C=	ENSP00000385794.2:n.*485C=
ENST00000647936.1:c.*619C=	ENSP00000496822.1:n.*619C=
ENST00000648381.1:n.2684C=
ENST00000648853.1:c.*485C=	ENSP00000497262.1:n.*485C=
ENST00000650591.1:c.*485C=	ENSP00000497376.1:n.*485C=
ENST00000394236.7:c.*485C=	ENSP00000377783.3:n.*485C=
ENST00000407433.5:c.*485C=	ENSP00000385794.1:n.*485C=
NM_000313.3:c.*485C= , LRG_572t1:c.*485C=	NP_000304.2:n.*485C=
NM_001314077.1:c.*485C= , LRG_572t2:c.*485C=	NP_001301006.1:n.*485C=
NM_000313.4:c.*485C= MANE Select	NP_000304.2:n.*485C=
NM_001314077.2:c.*485C=	NP_001301006.1:n.*485C=