Canonical Allele Identifier: CA1385036813

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892993A= , CM000665.2:g.93892993A=	GRCh38
NC_000003.11:g.93611837A= , CM000665.1:g.93611837A=	GRCh37
NC_000003.10:g.95094527A=	NCBI36
NG_009813.1:g.86098T= , LRG_572:g.86098T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1095T=	ENSP00000330021.7:p.Asn365=
ENST00000394236.9:c.1095T= MANE Select	ENSP00000377783.3:p.Asn365=
ENST00000407433.6:c.1050T=	ENSP00000385794.2:p.Asn350=
ENST00000647936.1:c.1095T=	ENSP00000496822.1:p.Asn365=
ENST00000648381.1:n.1263T=
ENST00000648853.1:c.1053T=	ENSP00000497262.1:p.Asn351=
ENST00000649103.1:c.1194T=	ENSP00000497962.1:n.1194T=
ENST00000650591.1:c.1191T=	ENSP00000497376.1:p.Asn397=
ENST00000394236.7:c.1095T=	ENSP00000377783.3:p.Asn365=
ENST00000407433.5:c.702T=	ENSP00000385794.1:p.Asn234=
NM_000313.3:c.1095T= , LRG_572t1:c.1095T=	NP_000304.2:p.Asn365=
NM_001314077.1:c.1191T= , LRG_572t2:c.1191T=	NP_001301006.1:p.Asn397=
NM_000313.4:c.1095T= MANE Select	NP_000304.2:p.Asn365=
NM_001314077.2:c.1191T=	NP_001301006.1:p.Asn397=