Canonical Allele Identifier: CA2333953297

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36066077_36066078delinsCT , CM000681.2:g.36066077_36066078delinsCT	GRCh38
NC_000019.9:g.36556979_36556980delinsCT , CM000681.1:g.36556979_36556980delinsCT	GRCh37
NC_000019.8:g.41248819_41248820delinsCT	NCBI36
NG_028101.1:g.16197_16198delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.390+62_390+63delinsCT	ENSP00000270301.6:n.390+62_390+63delinsCT
ENST00000401500.7:c.390+62_390+63delinsCT MANE Select	ENSP00000384792.1:n.390+62_390+63delinsCT
ENST00000427823.3:c.474+62_474+63delinsCT	ENSP00000413475.4:n.474+62_474+63delinsCT
ENST00000587391.6:c.390+62_390+63delinsCT	ENSP00000465525.1:n.390+62_390+63delinsCT
ENST00000589953.2:n.516_517delinsCT
ENST00000644764.2:c.390+62_390+63delinsCT	ENSP00000494253.2:n.390+62_390+63delinsCT
ENST00000679682.1:c.390+62_390+63delinsCT	ENSP00000506226.1:n.390+62_390+63delinsCT
ENST00000679714.1:c.390+62_390+63delinsCT	ENSP00000506627.1:n.390+62_390+63delinsCT
ENST00000679757.1:c.390+62_390+63delinsCT	ENSP00000505158.1:n.390+62_390+63delinsCT
ENST00000679858.1:c.390+62_390+63delinsCT	ENSP00000505655.1:n.390+62_390+63delinsCT
ENST00000680321.1:c.390+62_390+63delinsCT	ENSP00000505525.1:n.390+62_390+63delinsCT
ENST00000680359.1:c.390+62_390+63delinsCT	ENSP00000506079.1:n.390+62_390+63delinsCT
ENST00000680403.1:c.390+62_390+63delinsCT	ENSP00000505677.1:n.390+62_390+63delinsCT
ENST00000680489.1:n.713+62_713+63delinsCT
ENST00000680564.1:c.390+62_390+63delinsCT	ENSP00000505582.1:n.390+62_390+63delinsCT
ENST00000680590.1:c.390+62_390+63delinsCT	ENSP00000505350.1:n.390+62_390+63delinsCT
ENST00000680806.1:c.390+62_390+63delinsCT	ENSP00000506418.1:n.390+62_390+63delinsCT
ENST00000681542.1:c.390+62_390+63delinsCT	ENSP00000505251.1:n.390+62_390+63delinsCT
ENST00000681597.1:n.31_32delinsCT
ENST00000681625.1:c.390+62_390+63delinsCT	ENSP00000505555.1:n.390+62_390+63delinsCT
ENST00000681809.1:c.390+62_390+63delinsCT	ENSP00000505740.1:n.390+62_390+63delinsCT
ENST00000270301.11:c.390+62_390+63delinsCT	ENSP00000270301.6:n.390+62_390+63delinsCT
ENST00000378860.8:n.481+62_481+63delinsCT
ENST00000401500.6:c.390+62_390+63delinsCT	ENSP00000384792.1:n.390+62_390+63delinsCT
ENST00000427823.2:c.456+62_456+63delinsCT	ENSP00000413475.3:n.456+62_456+63delinsCT
ENST00000587391.5:c.390+62_390+63delinsCT	ENSP00000465525.1:n.390+62_390+63delinsCT
NM_001083961.1:c.390+62_390+63delinsCT	NP_001077430.1:n.390+62_390+63delinsCT
NM_173636.4:c.390+62_390+63delinsCT	NP_775907.4:n.390+62_390+63delinsCT
XM_005258809.2:c.390+62_390+63delinsCT	XP_005258866.1:n.390+62_390+63delinsCT
XM_011526837.1:c.390+62_390+63delinsCT	XP_011525139.1:n.390+62_390+63delinsCT
XM_011526838.1:c.390+62_390+63delinsCT	XP_011525140.1:n.390+62_390+63delinsCT
XM_011526839.1:c.390+62_390+63delinsCT	XP_011525141.1:n.390+62_390+63delinsCT
XM_017026665.1:c.390+62_390+63delinsCT	XP_016882154.1:n.390+62_390+63delinsCT
XR_001753671.1:n.481+62_481+63delinsCT
XR_001753672.1:n.481+62_481+63delinsCT
NM_001083961.2:c.390+62_390+63delinsCT MANE Select	NP_001077430.1:n.390+62_390+63delinsCT
NM_173636.5:c.390+62_390+63delinsCT	NP_775907.4:n.390+62_390+63delinsCT