Canonical Allele Identifier: CA1385039132

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898521T= , CM000665.2:g.93898521T=	GRCh38
NC_000003.11:g.93617365T= , CM000665.1:g.93617365T=	GRCh37
NC_000003.10:g.95100055T=	NCBI36
NG_009813.1:g.80570A= , LRG_572:g.80570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.776A=	ENSP00000330021.7:p.Tyr259=
ENST00000394236.9:c.776A= MANE Select	ENSP00000377783.3:p.Tyr259=
ENST00000407433.6:c.731A=	ENSP00000385794.2:p.Tyr244=
ENST00000647936.1:c.776A=	ENSP00000496822.1:p.Tyr259=
ENST00000648381.1:n.944A=
ENST00000648853.1:c.734A=	ENSP00000497262.1:p.Tyr245=
ENST00000649103.1:c.875A=	ENSP00000497962.1:n.875A=
ENST00000650591.1:c.872A=	ENSP00000497376.1:p.Tyr291=
ENST00000394236.7:c.776A=	ENSP00000377783.3:p.Tyr259=
ENST00000407433.5:c.383A=	ENSP00000385794.1:p.Tyr128=
NM_000313.3:c.776A= , LRG_572t1:c.776A=	NP_000304.2:p.Tyr259=
NM_001314077.1:c.872A= , LRG_572t2:c.872A=	NP_001301006.1:p.Tyr291=
NM_000313.4:c.776A= MANE Select	NP_000304.2:p.Tyr259=
NM_001314077.2:c.872A=	NP_001301006.1:p.Tyr291=