Canonical Allele Identifier: CA1385036837

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893045G= , CM000665.2:g.93893045G=	GRCh38
NC_000003.11:g.93611889G= , CM000665.1:g.93611889G=	GRCh37
NC_000003.10:g.95094579G=	NCBI36
NG_009813.1:g.86046C= , LRG_572:g.86046C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1043C=	ENSP00000330021.7:p.Ala348=
ENST00000394236.9:c.1043C= MANE Select	ENSP00000377783.3:p.Ala348=
ENST00000407433.6:c.998C=	ENSP00000385794.2:p.Ala333=
ENST00000647936.1:c.1043C=	ENSP00000496822.1:p.Ala348=
ENST00000648381.1:n.1211C=
ENST00000648853.1:c.1001C=	ENSP00000497262.1:p.Ala334=
ENST00000649103.1:c.1142C=	ENSP00000497962.1:n.1142C=
ENST00000650591.1:c.1139C=	ENSP00000497376.1:p.Ala380=
ENST00000394236.7:c.1043C=	ENSP00000377783.3:p.Ala348=
ENST00000407433.5:c.650C=	ENSP00000385794.1:p.Ala217=
NM_000313.3:c.1043C= , LRG_572t1:c.1043C=	NP_000304.2:p.Ala348=
NM_001314077.1:c.1139C= , LRG_572t2:c.1139C=	NP_001301006.1:p.Ala380=
NM_000313.4:c.1043C= MANE Select	NP_000304.2:p.Ala348=
NM_001314077.2:c.1139C=	NP_001301006.1:p.Ala380=