Canonical Allele Identifier: CA1385038300

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896597A= , CM000665.2:g.93896597A=	GRCh38
NC_000003.11:g.93615441A= , CM000665.1:g.93615441A=	GRCh37
NC_000003.10:g.95098131A=	NCBI36
NG_009813.1:g.82494T= , LRG_572:g.82494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.944T=	ENSP00000330021.7:p.Phe315=
ENST00000394236.9:c.944T= MANE Select	ENSP00000377783.3:p.Phe315=
ENST00000407433.6:c.899T=	ENSP00000385794.2:p.Phe300=
ENST00000647936.1:c.944T=	ENSP00000496822.1:p.Phe315=
ENST00000648381.1:n.1112T=
ENST00000648853.1:c.902T=	ENSP00000497262.1:p.Phe301=
ENST00000649103.1:c.1043T=	ENSP00000497962.1:n.1043T=
ENST00000650591.1:c.1040T=	ENSP00000497376.1:p.Phe347=
ENST00000394236.7:c.944T=	ENSP00000377783.3:p.Phe315=
ENST00000407433.5:c.551T=	ENSP00000385794.1:p.Phe184=
NM_000313.3:c.944T= , LRG_572t1:c.944T=	NP_000304.2:p.Phe315=
NM_001314077.1:c.1040T= , LRG_572t2:c.1040T=	NP_001301006.1:p.Phe347=
NM_000313.4:c.944T= MANE Select	NP_000304.2:p.Phe315=
NM_001314077.2:c.1040T=	NP_001301006.1:p.Phe347=