Canonical Allele Identifier: CA392199008

Gene: WDR76

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43861373C>A , CM000677.2:g.43861373C>A	GRCh38
NC_000015.9:g.44153571C>A , CM000677.1:g.44153571C>A	GRCh37
NC_000015.8:g.41940863C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024908.4:c.1603C>A MANE Select	NP_079184.2:p.Leu535Ile
ENST00000263795.11:c.1603C>A MANE Select	ENSP00000263795.6:p.Leu535Ile
NM_001167941.1:c.1411C>A	NP_001161413.1:p.Leu471Ile
NM_001167941.2:c.1411C>A	NP_001161413.1:p.Leu471Ile
NM_024908.3:c.1603C>A	NP_079184.2:p.Leu535Ile
ENST00000263795.10:c.1603C>A	ENSP00000263795.6:p.Leu535Ile
ENST00000381246.6:c.1411C>A	ENSP00000370645.2:p.Leu471Ile
ENST00000478130.1:n.268C>A
XM_005254680.2:c.1411C>A	XP_005254737.1:p.Leu471Ile
XM_005254680.3:c.1411C>A	XP_005254737.1:p.Leu471Ile
XR_001751398.2:n.1643C>A