Canonical Allele Identifier: CA9396217

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102724G>T , CM000681.2:g.36102724G>T	GRCh38
NC_000019.9:g.36593626G>T , CM000681.1:g.36593626G>T	GRCh37
NC_000019.8:g.41285466G>T	NCBI36
NG_028101.1:g.52844G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3221-28G>T	ENSP00000270301.6:n.3221-28G>T
ENST00000401500.7:c.3221-13G>T MANE Select	ENSP00000384792.1:n.3221-13G>T
ENST00000587391.6:c.*3068G>T	ENSP00000465525.1:n.*3068G>T
ENST00000679357.1:c.1288G>T
ENST00000679682.1:c.3206-13G>T	ENSP00000506226.1:n.3206-13G>T
ENST00000679714.1:c.3215-13G>T	ENSP00000506627.1:n.3215-13G>T
ENST00000679757.1:c.2870-13G>T	ENSP00000505158.1:n.2870-13G>T
ENST00000679858.1:c.*2603-13G>T	ENSP00000505655.1:n.*2603-13G>T
ENST00000680211.1:c.-179-13G>T	ENSP00000506102.1:n.-179-13G>T
ENST00000680280.1:n.495G>T
ENST00000680349.1:n.1776G>T
ENST00000680403.1:c.3221-28G>T	ENSP00000505677.1:n.3221-28G>T
ENST00000680564.1:c.2972-13G>T	ENSP00000505582.1:n.2972-13G>T
ENST00000680590.1:c.*1616-28G>T	ENSP00000505350.1:n.*1616-28G>T
ENST00000680739.1:c.236-13G>T
ENST00000680773.1:n.1709G>T
ENST00000680806.1:c.*2511G>T	ENSP00000506418.1:n.*2511G>T
ENST00000680997.1:n.1140G>T
ENST00000681608.1:n.741G>T
ENST00000681625.1:c.*553-13G>T	ENSP00000505555.1:n.*553-13G>T
ENST00000681648.1:n.507G>T
ENST00000270301.11:c.3221-28G>T	ENSP00000270301.6:n.3221-28G>T
ENST00000401500.6:c.3221-13G>T	ENSP00000384792.1:n.3221-13G>T
ENST00000587391.5:c.*3068G>T	ENSP00000465525.1:n.*3068G>T
NM_001083961.1:c.3221-13G>T	NP_001077430.1:n.3221-13G>T
NM_173636.4:c.3221-28G>T	NP_775907.4:n.3221-28G>T
XM_005258809.2:c.3110-13G>T	XP_005258866.1:n.3110-13G>T
XM_011526837.1:c.3206-13G>T	XP_011525139.1:n.3206-13G>T
XM_011526838.1:c.2972-13G>T	XP_011525140.1:n.2972-13G>T
XM_011526839.1:c.2870-13G>T	XP_011525141.1:n.2870-13G>T
XM_011526840.1:c.2213-13G>T	XP_011525142.1:n.2213-13G>T
XM_011526841.1:c.1799-13G>T	XP_011525143.1:n.1799-13G>T
XM_011526842.1:c.1652-13G>T	XP_011525144.1:n.1652-13G>T
XM_011526843.1:c.968-13G>T	XP_011525145.1:n.968-13G>T
XM_011526844.1:c.968-13G>T	XP_011525146.1:n.968-13G>T
XM_011526840.2:c.2213-13G>T	XP_011525142.1:n.2213-13G>T
XM_011526841.2:c.1799-13G>T	XP_011525143.1:n.1799-13G>T
XM_011526844.2:c.968-13G>T	XP_011525146.1:n.968-13G>T
XM_017026665.1:c.3221-13G>T	XP_016882154.1:n.3221-13G>T
NM_001083961.2:c.3221-13G>T MANE Select	NP_001077430.1:n.3221-13G>T
NM_173636.5:c.3221-28G>T	NP_775907.4:n.3221-28G>T