Canonical Allele Identifier: CA1385040185

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900825G= , CM000665.2:g.93900825G=	GRCh38
NC_000003.11:g.93619669G= , CM000665.1:g.93619669G=	GRCh37
NC_000003.10:g.95102359G=	NCBI36
NG_009813.1:g.78266C= , LRG_572:g.78266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.706C=	ENSP00000330021.7:p.Leu236=
ENST00000394236.9:c.706C= MANE Select	ENSP00000377783.3:p.Leu236=
ENST00000407433.6:c.661C=	ENSP00000385794.2:p.Leu221=
ENST00000647936.1:c.706C=	ENSP00000496822.1:p.Leu236=
ENST00000648381.1:n.874C=
ENST00000648853.1:c.664C=	ENSP00000497262.1:p.Leu222=
ENST00000649103.1:c.805C=	ENSP00000497962.1:n.805C=
ENST00000650591.1:c.802C=	ENSP00000497376.1:p.Leu268=
ENST00000394236.7:c.706C=	ENSP00000377783.3:p.Leu236=
ENST00000407433.5:c.313C=	ENSP00000385794.1:p.Leu105=
NM_000313.3:c.706C= , LRG_572t1:c.706C=	NP_000304.2:p.Leu236=
NM_001314077.1:c.802C= , LRG_572t2:c.802C=	NP_001301006.1:p.Leu268=
NM_000313.4:c.706C= MANE Select	NP_000304.2:p.Leu236=
NM_001314077.2:c.802C=	NP_001301006.1:p.Leu268=