Canonical Allele Identifier: CA1385036839

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893052G= , CM000665.2:g.93893052G=	GRCh38
NC_000003.11:g.93611896G= , CM000665.1:g.93611896G=	GRCh37
NC_000003.10:g.95094586G=	NCBI36
NG_009813.1:g.86039C= , LRG_572:g.86039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1036C=	ENSP00000330021.7:p.His346=
ENST00000394236.9:c.1036C= MANE Select	ENSP00000377783.3:p.His346=
ENST00000407433.6:c.991C=	ENSP00000385794.2:p.His331=
ENST00000647936.1:c.1036C=	ENSP00000496822.1:p.His346=
ENST00000648381.1:n.1204C=
ENST00000648853.1:c.994C=	ENSP00000497262.1:p.His332=
ENST00000649103.1:c.1135C=	ENSP00000497962.1:n.1135C=
ENST00000650591.1:c.1132C=	ENSP00000497376.1:p.His378=
ENST00000394236.7:c.1036C=	ENSP00000377783.3:p.His346=
ENST00000407433.5:c.643C=	ENSP00000385794.1:p.His215=
NM_000313.3:c.1036C= , LRG_572t1:c.1036C=	NP_000304.2:p.His346=
NM_001314077.1:c.1132C= , LRG_572t2:c.1132C=	NP_001301006.1:p.His378=
NM_000313.4:c.1036C= MANE Select	NP_000304.2:p.His346=
NM_001314077.2:c.1132C=	NP_001301006.1:p.His378=