Canonical Allele Identifier: CA307843459

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36105085G>A , CM000681.2:g.36105085G>A	GRCh38
NC_000019.9:g.36595987G>A , CM000681.1:g.36595987G>A	GRCh37
NC_000019.8:g.41287827G>A	NCBI36
NG_028101.1:g.55205G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4614G>A	ENSP00000270301.6:n.4614G>A
ENST00000401500.7:c.*57G>A MANE Select	ENSP00000384792.1:n.*57G>A
ENST00000587391.6:c.*4489G>A	ENSP00000465525.1:n.*4489G>A
ENST00000679598.1:c.1374G>A
ENST00000679682.1:c.*57G>A	ENSP00000506226.1:n.*57G>A
ENST00000679714.1:c.*57G>A	ENSP00000506627.1:n.*57G>A
ENST00000679757.1:c.*57G>A	ENSP00000505158.1:n.*57G>A
ENST00000679858.1:c.*4011G>A	ENSP00000505655.1:n.*4011G>A
ENST00000680211.1:c.*57G>A	ENSP00000506102.1:n.*57G>A
ENST00000680349.1:n.3278G>A
ENST00000680564.1:c.*57G>A	ENSP00000505582.1:n.*57G>A
ENST00000680590.1:c.*3009G>A	ENSP00000505350.1:n.*3009G>A
ENST00000680597.1:c.1362G>A
ENST00000680739.1:c.1644G>A
ENST00000680773.1:n.3130G>A
ENST00000270301.11:c.4614G>A	ENSP00000270301.6:n.4614G>A
ENST00000401500.6:c.*57G>A	ENSP00000384792.1:n.*57G>A
ENST00000587391.5:c.*4489G>A	ENSP00000465525.1:n.*4489G>A
NM_001083961.1:c.*57G>A	NP_001077430.1:n.*57G>A
NM_173636.4:c.*57G>A	NP_775907.4:n.*57G>A
XM_005258809.2:c.*57G>A	XP_005258866.1:n.*57G>A
XM_011526837.1:c.*57G>A	XP_011525139.1:n.*57G>A
XM_011526838.1:c.*57G>A	XP_011525140.1:n.*57G>A
XM_011526839.1:c.*57G>A	XP_011525141.1:n.*57G>A
XM_011526840.1:c.*57G>A	XP_011525142.1:n.*57G>A
XM_011526841.1:c.*57G>A	XP_011525143.1:n.*57G>A
XM_011526842.1:c.*57G>A	XP_011525144.1:n.*57G>A
XM_011526843.1:c.*57G>A	XP_011525145.1:n.*57G>A
XM_011526844.1:c.*57G>A	XP_011525146.1:n.*57G>A
XM_011526840.2:c.*57G>A	XP_011525142.1:n.*57G>A
XM_011526841.2:c.*57G>A	XP_011525143.1:n.*57G>A
XM_011526844.2:c.*57G>A	XP_011525146.1:n.*57G>A
XM_017026665.1:c.*45+12G>A	XP_016882154.1:n.*45+12G>A
NM_001083961.2:c.*57G>A MANE Select	NP_001077430.1:n.*57G>A
NM_173636.5:c.*57G>A	NP_775907.4:n.*57G>A