Canonical Allele Identifier: CA1385026912

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874286G= , CM000665.2:g.93874286G=	GRCh38
NC_000003.11:g.93593130G= , CM000665.1:g.93593130G=	GRCh37
NC_000003.10:g.95075820G=	NCBI36
NG_009813.1:g.104805C= , LRG_572:g.104805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1990C=	ENSP00000330021.7:p.His664=
ENST00000394236.9:c.1990C= MANE Select	ENSP00000377783.3:p.His664=
ENST00000407433.6:c.1945C=	ENSP00000385794.2:p.His649=
ENST00000647936.1:c.*93C=	ENSP00000496822.1:n.*93C=
ENST00000648381.1:n.2158C=
ENST00000648853.1:c.1948C=	ENSP00000497262.1:p.His650=
ENST00000650591.1:c.2086C=	ENSP00000497376.1:p.His696=
ENST00000394236.7:c.1990C=	ENSP00000377783.3:p.His664=
ENST00000407433.5:c.1597C=	ENSP00000385794.1:p.His533=
NM_000313.3:c.1990C= , LRG_572t1:c.1990C=	NP_000304.2:p.His664=
NM_001314077.1:c.2086C= , LRG_572t2:c.2086C=	NP_001301006.1:p.His696=
NM_000313.4:c.1990C= MANE Select	NP_000304.2:p.His664=
NM_001314077.2:c.2086C=	NP_001301006.1:p.His696=