Canonical Allele Identifier: CA1385033054

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93884769T= , CM000665.2:g.93884769T=	GRCh38
NC_000003.11:g.93603613T= , CM000665.1:g.93603613T=	GRCh37
NC_000003.10:g.95086303T=	NCBI36
NG_009813.1:g.94322A= , LRG_572:g.94322A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1451A=	ENSP00000330021.7:p.Tyr484=
ENST00000394236.9:c.1451A= MANE Select	ENSP00000377783.3:p.Tyr484=
ENST00000407433.6:c.1406A=	ENSP00000385794.2:p.Tyr469=
ENST00000647936.1:c.1451A=	ENSP00000496822.1:p.Tyr484=
ENST00000648381.1:n.1619A=
ENST00000648853.1:c.1409A=	ENSP00000497262.1:p.Tyr470=
ENST00000649103.1:c.1550A=	ENSP00000497962.1:n.1550A=
ENST00000649585.1:c.206A=	ENSP00000498163.1:p.Tyr69=
ENST00000650591.1:c.1547A=	ENSP00000497376.1:p.Tyr516=
ENST00000394236.7:c.1451A=	ENSP00000377783.3:p.Tyr484=
ENST00000407433.5:c.1058A=	ENSP00000385794.1:p.Tyr353=
NM_000313.3:c.1451A= , LRG_572t1:c.1451A=	NP_000304.2:p.Tyr484=
NM_001314077.1:c.1547A= , LRG_572t2:c.1547A=	NP_001301006.1:p.Tyr516=
NM_000313.4:c.1451A= MANE Select	NP_000304.2:p.Tyr484=
NM_001314077.2:c.1547A=	NP_001301006.1:p.Tyr516=