Canonical Allele Identifier: CA1385036799

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892966T= , CM000665.2:g.93892966T=	GRCh38
NC_000003.11:g.93611810T= , CM000665.1:g.93611810T=	GRCh37
NC_000003.10:g.95094500T=	NCBI36
NG_009813.1:g.86125A= , LRG_572:g.86125A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1122A=	ENSP00000330021.7:p.Gly374=
ENST00000394236.9:c.1122A= MANE Select	ENSP00000377783.3:p.Gly374=
ENST00000407433.6:c.1077A=	ENSP00000385794.2:p.Gly359=
ENST00000647936.1:c.1122A=	ENSP00000496822.1:p.Gly374=
ENST00000648381.1:n.1290A=
ENST00000648853.1:c.1080A=	ENSP00000497262.1:p.Gly360=
ENST00000649103.1:c.1221A=	ENSP00000497962.1:n.1221A=
ENST00000650591.1:c.1218A=	ENSP00000497376.1:p.Gly406=
ENST00000394236.7:c.1122A=	ENSP00000377783.3:p.Gly374=
ENST00000407433.5:c.729A=	ENSP00000385794.1:p.Gly243=
NM_000313.3:c.1122A= , LRG_572t1:c.1122A=	NP_000304.2:p.Gly374=
NM_001314077.1:c.1218A= , LRG_572t2:c.1218A=	NP_001301006.1:p.Gly406=
NM_000313.4:c.1122A= MANE Select	NP_000304.2:p.Gly374=
NM_001314077.2:c.1218A=	NP_001301006.1:p.Gly406=