Canonical Allele Identifier: CA9396299

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103162G>A , CM000681.2:g.36103162G>A	GRCh38
NC_000019.9:g.36594064G>A , CM000681.1:g.36594064G>A	GRCh37
NC_000019.8:g.41285904G>A	NCBI36
NG_028101.1:g.53282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3454G>A	ENSP00000270301.6:p.Ala1152Thr
ENST00000401500.7:c.3469G>A MANE Select	ENSP00000384792.1:p.Ala1157Thr
ENST00000587391.6:c.*3329G>A	ENSP00000465525.1:n.*3329G>A
ENST00000679357.1:c.1549G>A
ENST00000679598.1:c.234G>A
ENST00000679682.1:c.3454G>A	ENSP00000506226.1:p.Ala1152Thr
ENST00000679714.1:c.3463G>A	ENSP00000506627.1:p.Ala1155Thr
ENST00000679757.1:c.3118G>A	ENSP00000505158.1:p.Ala1040Thr
ENST00000679858.1:c.*2851G>A	ENSP00000505655.1:n.*2851G>A
ENST00000680211.1:c.70G>A	ENSP00000506102.1:p.Ala24Thr
ENST00000680280.1:n.837G>A
ENST00000680349.1:n.2118G>A
ENST00000680403.1:c.3454G>A	ENSP00000505677.1:p.Ala1152Thr
ENST00000680564.1:c.3220G>A	ENSP00000505582.1:p.Ala1074Thr
ENST00000680590.1:c.*1849G>A	ENSP00000505350.1:n.*1849G>A
ENST00000680597.1:c.202G>A
ENST00000680739.1:c.484G>A
ENST00000680773.1:n.1970G>A
ENST00000680806.1:c.*2772G>A	ENSP00000506418.1:n.*2772G>A
ENST00000680997.1:n.1401G>A
ENST00000681608.1:n.1179G>A
ENST00000681625.1:c.*801G>A	ENSP00000505555.1:n.*801G>A
ENST00000681648.1:n.849G>A
ENST00000270301.11:c.3454G>A	ENSP00000270301.6:p.Ala1152Thr
ENST00000401500.6:c.3469G>A	ENSP00000384792.1:p.Ala1157Thr
ENST00000587391.5:c.*3329G>A	ENSP00000465525.1:n.*3329G>A
NM_001083961.1:c.3469G>A	NP_001077430.1:p.Ala1157Thr
NM_173636.4:c.3454G>A	NP_775907.4:p.Ala1152Thr
XM_005258809.2:c.3358G>A	XP_005258866.1:p.Ala1120Thr
XM_011526837.1:c.3454G>A	XP_011525139.1:p.Ala1152Thr
XM_011526838.1:c.3220G>A	XP_011525140.1:p.Ala1074Thr
XM_011526839.1:c.3118G>A	XP_011525141.1:p.Ala1040Thr
XM_011526840.1:c.2461G>A	XP_011525142.1:p.Ala821Thr
XM_011526841.1:c.2047G>A	XP_011525143.1:p.Ala683Thr
XM_011526842.1:c.1900G>A	XP_011525144.1:p.Ala634Thr
XM_011526843.1:c.1216G>A	XP_011525145.1:p.Ala406Thr
XM_011526844.1:c.1216G>A	XP_011525146.1:p.Ala406Thr
XM_011526840.2:c.2461G>A	XP_011525142.1:p.Ala821Thr
XM_011526841.2:c.2047G>A	XP_011525143.1:p.Ala683Thr
XM_011526844.2:c.1216G>A	XP_011525146.1:p.Ala406Thr
XM_017026665.1:c.3469G>A	XP_016882154.1:p.Ala1157Thr
NM_001083961.2:c.3469G>A MANE Select	NP_001077430.1:p.Ala1157Thr
NM_173636.5:c.3454G>A	NP_775907.4:p.Ala1152Thr