Canonical Allele Identifier: CA1385036834

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893033A= , CM000665.2:g.93893033A=	GRCh38
NC_000003.11:g.93611877A= , CM000665.1:g.93611877A=	GRCh37
NC_000003.10:g.95094567A=	NCBI36
NG_009813.1:g.86058T= , LRG_572:g.86058T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1055T=	ENSP00000330021.7:p.Ile352=
ENST00000394236.9:c.1055T= MANE Select	ENSP00000377783.3:p.Ile352=
ENST00000407433.6:c.1010T=	ENSP00000385794.2:p.Ile337=
ENST00000647936.1:c.1055T=	ENSP00000496822.1:p.Ile352=
ENST00000648381.1:n.1223T=
ENST00000648853.1:c.1013T=	ENSP00000497262.1:p.Ile338=
ENST00000649103.1:c.1154T=	ENSP00000497962.1:n.1154T=
ENST00000650591.1:c.1151T=	ENSP00000497376.1:p.Ile384=
ENST00000394236.7:c.1055T=	ENSP00000377783.3:p.Ile352=
ENST00000407433.5:c.662T=	ENSP00000385794.1:p.Ile221=
NM_000313.3:c.1055T= , LRG_572t1:c.1055T=	NP_000304.2:p.Ile352=
NM_001314077.1:c.1151T= , LRG_572t2:c.1151T=	NP_001301006.1:p.Ile384=
NM_000313.4:c.1055T= MANE Select	NP_000304.2:p.Ile352=
NM_001314077.2:c.1151T=	NP_001301006.1:p.Ile384=