Canonical Allele Identifier: CA1385028980

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877069T= , CM000665.2:g.93877069T=	GRCh38
NC_000003.11:g.93595913T= , CM000665.1:g.93595913T=	GRCh37
NC_000003.10:g.95078603T=	NCBI36
NG_009813.1:g.102022A= , LRG_572:g.102022A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1767A=	ENSP00000330021.7:p.Pro589=
ENST00000394236.9:c.1767A= MANE Select	ENSP00000377783.3:p.Pro589=
ENST00000407433.6:c.1722A=	ENSP00000385794.2:p.Pro574=
ENST00000647936.1:c.1644+2094A=	ENSP00000496822.1:n.1644+2094A=
ENST00000648381.1:n.1935A=
ENST00000648853.1:c.1725A=	ENSP00000497262.1:p.Pro575=
ENST00000649103.1:c.1866A=	ENSP00000497962.1:n.1866A=
ENST00000649585.1:c.710A=	ENSP00000498163.1:n.710A=
ENST00000650591.1:c.1863A=	ENSP00000497376.1:p.Pro621=
ENST00000394236.7:c.1767A=	ENSP00000377783.3:p.Pro589=
ENST00000407433.5:c.1374A=	ENSP00000385794.1:p.Pro458=
NM_000313.3:c.1767A= , LRG_572t1:c.1767A=	NP_000304.2:p.Pro589=
NM_001314077.1:c.1863A= , LRG_572t2:c.1863A=	NP_001301006.1:p.Pro621=
NM_000313.4:c.1767A= MANE Select	NP_000304.2:p.Pro589=
NM_001314077.2:c.1863A=	NP_001301006.1:p.Pro621=