Canonical Allele Identifier: CA1385040182

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900822T= , CM000665.2:g.93900822T=	GRCh38
NC_000003.11:g.93619666T= , CM000665.1:g.93619666T=	GRCh37
NC_000003.10:g.95102356T=	NCBI36
NG_009813.1:g.78269A= , LRG_572:g.78269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.709A=	ENSP00000330021.7:p.Lys237=
ENST00000394236.9:c.709A= MANE Select	ENSP00000377783.3:p.Lys237=
ENST00000407433.6:c.664A=	ENSP00000385794.2:p.Lys222=
ENST00000647936.1:c.709A=	ENSP00000496822.1:p.Lys237=
ENST00000648381.1:n.877A=
ENST00000648853.1:c.667A=	ENSP00000497262.1:p.Lys223=
ENST00000649103.1:c.808A=	ENSP00000497962.1:n.808A=
ENST00000650591.1:c.805A=	ENSP00000497376.1:p.Lys269=
ENST00000394236.7:c.709A=	ENSP00000377783.3:p.Lys237=
ENST00000407433.5:c.316A=	ENSP00000385794.1:p.Lys106=
NM_000313.3:c.709A= , LRG_572t1:c.709A=	NP_000304.2:p.Lys237=
NM_001314077.1:c.805A= , LRG_572t2:c.805A=	NP_001301006.1:p.Lys269=
NM_000313.4:c.709A= MANE Select	NP_000304.2:p.Lys237=
NM_001314077.2:c.805A=	NP_001301006.1:p.Lys269=