Canonical Allele Identifier: CA1385028966

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877056T= , CM000665.2:g.93877056T=	GRCh38
NC_000003.11:g.93595900T= , CM000665.1:g.93595900T=	GRCh37
NC_000003.10:g.95078590T=	NCBI36
NG_009813.1:g.102035A= , LRG_572:g.102035A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1780A=	ENSP00000330021.7:p.Thr594=
ENST00000394236.9:c.1780A= MANE Select	ENSP00000377783.3:p.Thr594=
ENST00000407433.6:c.1735A=	ENSP00000385794.2:p.Thr579=
ENST00000647936.1:c.1644+2107A=	ENSP00000496822.1:n.1644+2107A=
ENST00000648381.1:n.1948A=
ENST00000648853.1:c.1738A=	ENSP00000497262.1:p.Thr580=
ENST00000649103.1:c.1879A=	ENSP00000497962.1:n.1879A=
ENST00000649585.1:c.723A=	ENSP00000498163.1:n.723A=
ENST00000650591.1:c.1876A=	ENSP00000497376.1:p.Thr626=
ENST00000394236.7:c.1780A=	ENSP00000377783.3:p.Thr594=
ENST00000407433.5:c.1387A=	ENSP00000385794.1:p.Thr463=
NM_000313.3:c.1780A= , LRG_572t1:c.1780A=	NP_000304.2:p.Thr594=
NM_001314077.1:c.1876A= , LRG_572t2:c.1876A=	NP_001301006.1:p.Thr626=
NM_000313.4:c.1780A= MANE Select	NP_000304.2:p.Thr594=
NM_001314077.2:c.1876A=	NP_001301006.1:p.Thr626=