Canonical Allele Identifier: CA405436905

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36083099C>G , CM000681.2:g.36083099C>G	GRCh38
NC_000019.9:g.36574001C>G , CM000681.1:g.36574001C>G	GRCh37
NC_000019.8:g.41265841C>G	NCBI36
NG_028101.1:g.33219C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001083961.2:c.1408C>G MANE Select	NP_001077430.1:p.Gln470Glu
ENST00000401500.7:c.1408C>G MANE Select	ENSP00000384792.1:p.Gln470Glu
NM_001083961.1:c.1408C>G	NP_001077430.1:p.Gln470Glu
NM_173636.4:c.1408C>G	NP_775907.4:p.Gln470Glu
NM_173636.5:c.1408C>G	NP_775907.4:p.Gln470Glu
ENST00000270301.11:c.1408C>G	ENSP00000270301.6:p.Gln470Glu
ENST00000270301.12:c.1408C>G	ENSP00000270301.6:p.Gln470Glu
ENST00000401500.6:c.1408C>G	ENSP00000384792.1:p.Gln470Glu
ENST00000587391.5:c.*98C>G	ENSP00000465525.1:n.*98C>G
ENST00000587391.6:c.*98C>G	ENSP00000465525.1:n.*98C>G
ENST00000644764.2:c.*200C>G	ENSP00000494253.2:n.*200C>G
ENST00000679682.1:c.1393C>G	ENSP00000506226.1:p.Gln465Glu
ENST00000679714.1:c.1402C>G	ENSP00000506627.1:p.Gln468Glu
ENST00000679757.1:c.1057C>G	ENSP00000505158.1:p.Gln353Glu
ENST00000679858.1:c.*205C>G	ENSP00000505655.1:n.*205C>G
ENST00000680359.1:c.1408C>G	ENSP00000506079.1:p.Gln470Glu
ENST00000680403.1:c.1408C>G	ENSP00000505677.1:p.Gln470Glu
ENST00000680489.1:n.1731C>G
ENST00000680564.1:c.1408C>G	ENSP00000505582.1:p.Gln470Glu
ENST00000680590.1:c.1408C>G	ENSP00000505350.1:p.Gln470Glu
ENST00000680806.1:c.*237C>G	ENSP00000506418.1:n.*237C>G
ENST00000681625.1:c.1393C>G	ENSP00000505555.1:p.Gln465Glu
XM_005258809.2:c.1408C>G	XP_005258866.1:p.Gln470Glu
XM_011526837.1:c.1393C>G	XP_011525139.1:p.Gln465Glu
XM_011526838.1:c.1408C>G	XP_011525140.1:p.Gln470Glu
XM_011526839.1:c.1057C>G	XP_011525141.1:p.Gln353Glu
XM_011526840.1:c.400C>G	XP_011525142.1:p.Gln134Glu
XM_011526840.2:c.400C>G	XP_011525142.1:p.Gln134Glu
XM_011526841.1:c.-15C>G	XP_011525143.1:n.-15C>G
XM_011526841.2:c.-15C>G	XP_011525143.1:n.-15C>G
XM_017026665.1:c.1408C>G	XP_016882154.1:p.Gln470Glu
XR_001753671.1:n.1499C>G
XR_001753672.1:n.1499C>G