Canonical Allele Identifier: CA2838301847

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36066023dup , CM000681.2:g.36066023dup	GRCh38
NC_000019.9:g.36556925dup , CM000681.1:g.36556925dup	GRCh37
NC_000019.8:g.41248765dup	NCBI36
NG_028101.1:g.16143dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.390+8dup	ENSP00000270301.6:n.390+8dup
ENST00000401500.7:c.390+8dup MANE Select	ENSP00000384792.1:n.390+8dup
ENST00000427823.3:c.474+8dup	ENSP00000413475.4:n.474+8dup
ENST00000587391.6:c.390+8dup	ENSP00000465525.1:n.390+8dup
ENST00000589953.2:n.462dup
ENST00000644764.2:c.390+8dup	ENSP00000494253.2:n.390+8dup
ENST00000679682.1:c.390+8dup	ENSP00000506226.1:n.390+8dup
ENST00000679714.1:c.390+8dup	ENSP00000506627.1:n.390+8dup
ENST00000679757.1:c.390+8dup	ENSP00000505158.1:n.390+8dup
ENST00000679858.1:c.390+8dup	ENSP00000505655.1:n.390+8dup
ENST00000680321.1:c.390+8dup	ENSP00000505525.1:n.390+8dup
ENST00000680359.1:c.390+8dup	ENSP00000506079.1:n.390+8dup
ENST00000680403.1:c.390+8dup	ENSP00000505677.1:n.390+8dup
ENST00000680489.1:n.713+8dup
ENST00000680564.1:c.390+8dup	ENSP00000505582.1:n.390+8dup
ENST00000680590.1:c.390+8dup	ENSP00000505350.1:n.390+8dup
ENST00000680806.1:c.390+8dup	ENSP00000506418.1:n.390+8dup
ENST00000681542.1:c.390+8dup	ENSP00000505251.1:n.390+8dup
ENST00000681625.1:c.390+8dup	ENSP00000505555.1:n.390+8dup
ENST00000681809.1:c.390+8dup	ENSP00000505740.1:n.390+8dup
ENST00000270301.11:c.390+8dup	ENSP00000270301.6:n.390+8dup
ENST00000378860.8:n.481+8dup
ENST00000401500.6:c.390+8dup	ENSP00000384792.1:n.390+8dup
ENST00000427823.2:c.456+8dup	ENSP00000413475.3:n.456+8dup
ENST00000587391.5:c.390+8dup	ENSP00000465525.1:n.390+8dup
NM_001083961.1:c.390+8dup	NP_001077430.1:n.390+8dup
NM_173636.4:c.390+8dup	NP_775907.4:n.390+8dup
XM_005258809.2:c.390+8dup	XP_005258866.1:n.390+8dup
XM_011526837.1:c.390+8dup	XP_011525139.1:n.390+8dup
XM_011526838.1:c.390+8dup	XP_011525140.1:n.390+8dup
XM_011526839.1:c.390+8dup	XP_011525141.1:n.390+8dup
XM_017026665.1:c.390+8dup	XP_016882154.1:n.390+8dup
XR_001753671.1:n.481+8dup
XR_001753672.1:n.481+8dup
NM_001083961.2:c.390+8dup MANE Select	NP_001077430.1:n.390+8dup
NM_173636.5:c.390+8dup	NP_775907.4:n.390+8dup