Canonical Allele Identifier: CA9395691

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36086740G>A , CM000681.2:g.36086740G>A	GRCh38
NC_000019.9:g.36577642G>A , CM000681.1:g.36577642G>A	GRCh37
NC_000019.8:g.41269482G>A	NCBI36
NG_028101.1:g.36860G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.1696G>A	ENSP00000270301.6:p.Val566Met
ENST00000401500.7:c.1696G>A MANE Select	ENSP00000384792.1:p.Val566Met
ENST00000587391.6:c.*386G>A	ENSP00000465525.1:n.*386G>A
ENST00000679489.1:c.54G>A
ENST00000679682.1:c.1681G>A	ENSP00000506226.1:p.Val561Met
ENST00000679714.1:c.1690G>A	ENSP00000506627.1:p.Val564Met
ENST00000679757.1:c.1345G>A	ENSP00000505158.1:p.Val449Met
ENST00000679858.1:c.*493G>A	ENSP00000505655.1:n.*493G>A
ENST00000680359.1:c.1696G>A	ENSP00000506079.1:p.Val566Met
ENST00000680377.1:c.146G>A
ENST00000680403.1:c.1696G>A	ENSP00000505677.1:p.Val566Met
ENST00000680489.1:n.2019G>A
ENST00000680564.1:c.1696G>A	ENSP00000505582.1:p.Val566Met
ENST00000680590.1:c.*95G>A	ENSP00000505350.1:n.*95G>A
ENST00000680806.1:c.*525G>A	ENSP00000506418.1:n.*525G>A
ENST00000680858.1:c.146G>A
ENST00000681302.1:c.146G>A
ENST00000681625.1:c.1681G>A	ENSP00000505555.1:p.Val561Met
ENST00000270301.11:c.1696G>A	ENSP00000270301.6:p.Val566Met
ENST00000401500.6:c.1696G>A	ENSP00000384792.1:p.Val566Met
ENST00000587391.5:c.*386G>A	ENSP00000465525.1:n.*386G>A
NM_001083961.1:c.1696G>A	NP_001077430.1:p.Val566Met
NM_173636.4:c.1696G>A	NP_775907.4:p.Val566Met
XM_005258809.2:c.1696G>A	XP_005258866.1:p.Val566Met
XM_011526837.1:c.1681G>A	XP_011525139.1:p.Val561Met
XM_011526838.1:c.1696G>A	XP_011525140.1:p.Val566Met
XM_011526839.1:c.1345G>A	XP_011525141.1:p.Val449Met
XM_011526840.1:c.688G>A	XP_011525142.1:p.Val230Met
XM_011526841.1:c.274G>A	XP_011525143.1:p.Val92Met
XM_011526842.1:c.127G>A	XP_011525144.1:p.Val43Met
XM_011526840.2:c.688G>A	XP_011525142.1:p.Val230Met
XM_011526841.2:c.274G>A	XP_011525143.1:p.Val92Met
XM_017026665.1:c.1696G>A	XP_016882154.1:p.Val566Met
XR_001753671.1:n.1787G>A
XR_001753672.1:n.1787G>A
NM_001083961.2:c.1696G>A MANE Select	NP_001077430.1:p.Val566Met
NM_173636.5:c.1696G>A	NP_775907.4:p.Val566Met