Canonical Allele Identifier: CA1385030672

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879362G= , CM000665.2:g.93879362G=	GRCh38
NC_000003.11:g.93598206G= , CM000665.1:g.93598206G=	GRCh37
NC_000003.10:g.95080896G=	NCBI36
NG_009813.1:g.99729C= , LRG_572:g.99729C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493-48C=	ENSP00000330021.7:n.1493-48C=
ENST00000394236.9:c.1493-48C= MANE Select	ENSP00000377783.3:n.1493-48C=
ENST00000407433.6:c.1448-48C=	ENSP00000385794.2:n.1448-48C=
ENST00000647936.1:c.1493-48C=	ENSP00000496822.1:n.1493-48C=
ENST00000648381.1:n.1661-48C=
ENST00000648853.1:c.1451-48C=	ENSP00000497262.1:n.1451-48C=
ENST00000649103.1:c.1592-48C=	ENSP00000497962.1:n.1592-48C=
ENST00000649585.1:c.436-48C=	ENSP00000498163.1:n.436-48C=
ENST00000650591.1:c.1589-48C=	ENSP00000497376.1:n.1589-48C=
ENST00000394236.7:c.1493-48C=	ENSP00000377783.3:n.1493-48C=
ENST00000407433.5:c.1100-48C=	ENSP00000385794.1:n.1100-48C=
NM_000313.3:c.1493-48C= , LRG_572t1:c.1493-48C=	NP_000304.2:n.1493-48C=
NM_001314077.1:c.1589-48C= , LRG_572t2:c.1589-48C=	NP_001301006.1:n.1589-48C=
NM_000313.4:c.1493-48C= MANE Select	NP_000304.2:n.1493-48C=
NM_001314077.2:c.1589-48C=	NP_001301006.1:n.1589-48C=