Canonical Allele Identifier: CA1385026937

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874347A= , CM000665.2:g.93874347A=	GRCh38
NC_000003.11:g.93593191A= , CM000665.1:g.93593191A=	GRCh37
NC_000003.10:g.95075881A=	NCBI36
NG_009813.1:g.104744T= , LRG_572:g.104744T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1929T=	ENSP00000330021.7:p.Asn643=
ENST00000394236.9:c.1929T= MANE Select	ENSP00000377783.3:p.Asn643=
ENST00000407433.6:c.1884T=	ENSP00000385794.2:p.Asn628=
ENST00000647936.1:c.*32T=	ENSP00000496822.1:n.*32T=
ENST00000648381.1:n.2097T=
ENST00000648853.1:c.1887T=	ENSP00000497262.1:p.Asn629=
ENST00000650591.1:c.2025T=	ENSP00000497376.1:p.Asn675=
ENST00000394236.7:c.1929T=	ENSP00000377783.3:p.Asn643=
ENST00000407433.5:c.1536T=	ENSP00000385794.1:p.Asn512=
NM_000313.3:c.1929T= , LRG_572t1:c.1929T=	NP_000304.2:p.Asn643=
NM_001314077.1:c.2025T= , LRG_572t2:c.2025T=	NP_001301006.1:p.Asn675=
NM_000313.4:c.1929T= MANE Select	NP_000304.2:p.Asn643=
NM_001314077.2:c.2025T=	NP_001301006.1:p.Asn675=