Canonical Allele Identifier: CA1385042504

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905656A= , CM000665.2:g.93905656A=	GRCh38
NC_000003.11:g.93624500A= , CM000665.1:g.93624500A=	GRCh37
NC_000003.10:g.95107190A=	NCBI36
NG_009813.1:g.73435T= , LRG_572:g.73435T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.601+128T=	ENSP00000330021.7:n.601+128T=
ENST00000394236.9:c.601+128T= MANE Select	ENSP00000377783.3:n.601+128T=
ENST00000407433.6:c.556+173T=	ENSP00000385794.2:n.556+173T=
ENST00000647936.1:c.601+128T=	ENSP00000496822.1:n.601+128T=
ENST00000648381.1:n.769+128T=
ENST00000648853.1:c.559+128T=	ENSP00000497262.1:n.559+128T=
ENST00000649103.1:c.700+128T=	ENSP00000497962.1:n.700+128T=
ENST00000650591.1:c.697+128T=	ENSP00000497376.1:n.697+128T=
ENST00000394236.7:c.601+128T=	ENSP00000377783.3:n.601+128T=
ENST00000407433.5:c.208+128T=	ENSP00000385794.1:n.208+128T=
NM_000313.3:c.601+128T= , LRG_572t1:c.601+128T=	NP_000304.2:n.601+128T=
NM_001314077.1:c.697+128T= , LRG_572t2:c.697+128T=	NP_001301006.1:n.697+128T=
NM_000313.4:c.601+128T= MANE Select	NP_000304.2:n.601+128T=
NM_001314077.2:c.697+128T=	NP_001301006.1:n.697+128T=