Canonical Allele Identifier: CA1385026935

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874342T= , CM000665.2:g.93874342T=	GRCh38
NC_000003.11:g.93593186T= , CM000665.1:g.93593186T=	GRCh37
NC_000003.10:g.95075876T=	NCBI36
NG_009813.1:g.104749A= , LRG_572:g.104749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1934A=	ENSP00000330021.7:p.Asn645=
ENST00000394236.9:c.1934A= MANE Select	ENSP00000377783.3:p.Asn645=
ENST00000407433.6:c.1889A=	ENSP00000385794.2:p.Asn630=
ENST00000647936.1:c.*37A=	ENSP00000496822.1:n.*37A=
ENST00000648381.1:n.2102A=
ENST00000648853.1:c.1892A=	ENSP00000497262.1:p.Asn631=
ENST00000650591.1:c.2030A=	ENSP00000497376.1:p.Asn677=
ENST00000394236.7:c.1934A=	ENSP00000377783.3:p.Asn645=
ENST00000407433.5:c.1541A=	ENSP00000385794.1:p.Asn514=
NM_000313.3:c.1934A= , LRG_572t1:c.1934A=	NP_000304.2:p.Asn645=
NM_001314077.1:c.2030A= , LRG_572t2:c.2030A=	NP_001301006.1:p.Asn677=
NM_000313.4:c.1934A= MANE Select	NP_000304.2:p.Asn645=
NM_001314077.2:c.2030A=	NP_001301006.1:p.Asn677=