Canonical Allele Identifier: CA1385039147

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898576T= , CM000665.2:g.93898576T=	GRCh38
NC_000003.11:g.93617420T= , CM000665.1:g.93617420T=	GRCh37
NC_000003.10:g.95100110T=	NCBI36
NG_009813.1:g.80515A= , LRG_572:g.80515A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.728-7A=	ENSP00000330021.7:n.728-7A=
ENST00000394236.9:c.728-7A= MANE Select	ENSP00000377783.3:n.728-7A=
ENST00000407433.6:c.683-7A=	ENSP00000385794.2:n.683-7A=
ENST00000647936.1:c.728-7A=	ENSP00000496822.1:n.728-7A=
ENST00000648381.1:n.896-7A=
ENST00000648853.1:c.686-7A=	ENSP00000497262.1:n.686-7A=
ENST00000649103.1:c.827-7A=	ENSP00000497962.1:n.827-7A=
ENST00000650591.1:c.824-7A=	ENSP00000497376.1:n.824-7A=
ENST00000394236.7:c.728-7A=	ENSP00000377783.3:n.728-7A=
ENST00000407433.5:c.335-7A=	ENSP00000385794.1:n.335-7A=
NM_000313.3:c.728-7A= , LRG_572t1:c.728-7A=	NP_000304.2:n.728-7A=
NM_001314077.1:c.824-7A= , LRG_572t2:c.824-7A=	NP_001301006.1:n.824-7A=
NM_000313.4:c.728-7A= MANE Select	NP_000304.2:n.728-7A=
NM_001314077.2:c.824-7A=	NP_001301006.1:n.824-7A=