Canonical Allele Identifier: CA1385036785

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892933C= , CM000665.2:g.93892933C=	GRCh38
NC_000003.11:g.93611777C= , CM000665.1:g.93611777C=	GRCh37
NC_000003.10:g.95094467C=	NCBI36
NG_009813.1:g.86158G= , LRG_572:g.86158G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1155G=	ENSP00000330021.7:p.Met385=
ENST00000394236.9:c.1155G= MANE Select	ENSP00000377783.3:p.Met385=
ENST00000407433.6:c.1110G=	ENSP00000385794.2:p.Met370=
ENST00000647936.1:c.1155G=	ENSP00000496822.1:p.Met385=
ENST00000648381.1:n.1323G=
ENST00000648853.1:c.1113G=	ENSP00000497262.1:p.Met371=
ENST00000649103.1:c.1254G=	ENSP00000497962.1:n.1254G=
ENST00000650591.1:c.1251G=	ENSP00000497376.1:p.Met417=
ENST00000394236.7:c.1155G=	ENSP00000377783.3:p.Met385=
ENST00000407433.5:c.762G=	ENSP00000385794.1:p.Met254=
NM_000313.3:c.1155G= , LRG_572t1:c.1155G=	NP_000304.2:p.Met385=
NM_001314077.1:c.1251G= , LRG_572t2:c.1251G=	NP_001301006.1:p.Met417=
NM_000313.4:c.1155G= MANE Select	NP_000304.2:p.Met385=
NM_001314077.2:c.1251G=	NP_001301006.1:p.Met417=