Canonical Allele Identifier: CA122001

Gene: PLAU C10orf55

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.73913343T= , CM000672.2:g.73913343T=	GRCh38
NC_000010.10:g.75673101T= , CM000672.1:g.75673101T=	GRCh37
NC_000010.9:g.75343107T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002658.6:c.422T= (PLAU) MANE Select	NP_002649.2:p.Leu141=
ENST00000372764.4:c.422T= (PLAU) MANE Select	ENSP00000361850.3:p.Leu141=
NM_001001791.2:c.-73-268A= (C10orf55)	NP_001001791.2:n.-73-268A=
NM_001145031.3:c.371T= (PLAU)	NP_001138503.2:p.Leu124=
NM_001319191.2:c.164T= (PLAU)	NP_001306120.2:p.Leu55=
NR_160937.1:n.320-268A= (C10orf55)
NR_160938.1:n.269-268A= (C10orf55)
ENST00000372764.3:c.422T= (PLAU)	ENSP00000361850.3:p.Leu141=
ENST00000409178.5:n.269-268A= (C10orf55)
ENST00000412307.3:c.-73-268A= (C10orf55)	ENSP00000409225.2:n.-73-268A=
ENST00000446342.5:c.371T= (PLAU)	ENSP00000388474.1:p.Leu124=
ENST00000494287.1:n.497T= (PLAU)
XM_011539866.1:c.422T= (PLAU)	XP_011538168.1:p.Leu141=
XM_011539866.2:c.422T= (PLAU)	XP_011538168.1:p.Leu141=
XM_011539867.1:c.164T= (PLAU)	XP_011538169.1:p.Leu55=