Canonical Allele Identifier: CA9395520

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36073542C>A , CM000681.2:g.36073542C>A	GRCh38
NC_000019.9:g.36564444C>A , CM000681.1:g.36564444C>A	GRCh37
NC_000019.8:g.41256284C>A	NCBI36
NG_028101.1:g.23662C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.1233+11C>A	ENSP00000270301.6:n.1233+11C>A
ENST00000401500.7:c.1233+11C>A MANE Select	ENSP00000384792.1:n.1233+11C>A
ENST00000587391.6:c.1233+11C>A	ENSP00000465525.1:n.1233+11C>A
ENST00000589953.2:n.1538+11C>A
ENST00000644764.2:c.1233+11C>A	ENSP00000494253.2:n.1233+11C>A
ENST00000679682.1:c.1218+11C>A	ENSP00000506226.1:n.1218+11C>A
ENST00000679714.1:c.1227+17C>A	ENSP00000506627.1:n.1227+17C>A
ENST00000679757.1:c.882+5532C>A	ENSP00000505158.1:n.882+5532C>A
ENST00000679858.1:c.*97+11C>A	ENSP00000505655.1:n.*97+11C>A
ENST00000680321.1:c.1218+11C>A	ENSP00000505525.1:n.1218+11C>A
ENST00000680359.1:c.1233+11C>A	ENSP00000506079.1:n.1233+11C>A
ENST00000680403.1:c.1233+11C>A	ENSP00000505677.1:n.1233+11C>A
ENST00000680489.1:n.1556+11C>A
ENST00000680564.1:c.1233+11C>A	ENSP00000505582.1:n.1233+11C>A
ENST00000680590.1:c.1233+11C>A	ENSP00000505350.1:n.1233+11C>A
ENST00000680806.1:c.1233+11C>A	ENSP00000506418.1:n.1233+11C>A
ENST00000681542.1:c.1233+11C>A	ENSP00000505251.1:n.1233+11C>A
ENST00000681625.1:c.1218+11C>A	ENSP00000505555.1:n.1218+11C>A
ENST00000270301.11:c.1233+11C>A	ENSP00000270301.6:n.1233+11C>A
ENST00000378860.8:n.1324+11C>A
ENST00000401500.6:c.1233+11C>A	ENSP00000384792.1:n.1233+11C>A
ENST00000587391.5:c.1233+11C>A	ENSP00000465525.1:n.1233+11C>A
ENST00000589953.1:n.301+11C>A
NM_001083961.1:c.1233+11C>A	NP_001077430.1:n.1233+11C>A
NM_173636.4:c.1233+11C>A	NP_775907.4:n.1233+11C>A
XM_005258809.2:c.1233+11C>A	XP_005258866.1:n.1233+11C>A
XM_011526837.1:c.1218+11C>A	XP_011525139.1:n.1218+11C>A
XM_011526838.1:c.1233+11C>A	XP_011525140.1:n.1233+11C>A
XM_011526839.1:c.882+5532C>A	XP_011525141.1:n.882+5532C>A
XM_011526840.1:c.74+11C>A	XP_011525142.1:n.74+11C>A
XM_011526840.2:c.74+11C>A	XP_011525142.1:n.74+11C>A
XM_017026665.1:c.1233+11C>A	XP_016882154.1:n.1233+11C>A
XR_001753671.1:n.1324+11C>A
XR_001753672.1:n.1324+11C>A
NM_001083961.2:c.1233+11C>A MANE Select	NP_001077430.1:n.1233+11C>A
NM_173636.5:c.1233+11C>A	NP_775907.4:n.1233+11C>A