Canonical Allele Identifier: CA995510552
Gene: WDR62 HGNC NCBI

Linked Data

dbSNP Id: rs1973594257

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104237G>A , CM000681.2:g.36104237G>A GRCh38
NC_000019.9:g.36595139G>A , CM000681.1:g.36595139G>A GRCh37
NC_000019.8:g.41286979G>A NCBI36
NG_028101.1:g.54357G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4138+256G>A ENSP00000270301.6:n.4138+256G>A
ENST00000401500.7:c.4153+256G>A MANE Select ENSP00000384792.1:n.4153+256G>A
ENST00000587391.6:c.*4013+256G>A ENSP00000465525.1:n.*4013+256G>A
ENST00000679357.1:c.2233+256G>A
ENST00000679598.1:c.918+256G>A
ENST00000679682.1:c.4138+256G>A ENSP00000506226.1:n.4138+256G>A
ENST00000679714.1:c.4147+256G>A ENSP00000506627.1:n.4147+256G>A
ENST00000679757.1:c.3802+256G>A ENSP00000505158.1:n.3802+256G>A
ENST00000679858.1:c.*3535+256G>A ENSP00000505655.1:n.*3535+256G>A
ENST00000680211.1:c.754+256G>A ENSP00000506102.1:n.754+256G>A
ENST00000680280.1:n.1656+256G>A
ENST00000680349.1:n.2802+256G>A
ENST00000680403.1:c.4138+256G>A ENSP00000505677.1:n.4138+256G>A
ENST00000680564.1:c.3904+256G>A ENSP00000505582.1:n.3904+256G>A
ENST00000680590.1:c.*2533+256G>A ENSP00000505350.1:n.*2533+256G>A
ENST00000680597.1:c.886+256G>A
ENST00000680739.1:c.1168+256G>A
ENST00000680773.1:n.2654+256G>A
ENST00000680806.1:c.*3456+256G>A ENSP00000506418.1:n.*3456+256G>A
ENST00000680997.1:n.2085+256G>A
ENST00000681608.1:n.1998+256G>A
ENST00000681625.1:c.*1485+256G>A ENSP00000505555.1:n.*1485+256G>A
ENST00000681648.1:n.1924G>A
ENST00000270301.11:c.4138+256G>A ENSP00000270301.6:n.4138+256G>A
ENST00000401500.6:c.4153+256G>A ENSP00000384792.1:n.4153+256G>A
ENST00000587391.5:c.*4013+256G>A ENSP00000465525.1:n.*4013+256G>A
NM_001083961.1:c.4153+256G>A NP_001077430.1:n.4153+256G>A
NM_173636.4:c.4138+256G>A NP_775907.4:n.4138+256G>A
XM_005258809.2:c.4042+256G>A XP_005258866.1:n.4042+256G>A
XM_011526837.1:c.4138+256G>A XP_011525139.1:n.4138+256G>A
XM_011526838.1:c.3904+256G>A XP_011525140.1:n.3904+256G>A
XM_011526839.1:c.3802+256G>A XP_011525141.1:n.3802+256G>A
XM_011526840.1:c.3145+256G>A XP_011525142.1:n.3145+256G>A
XM_011526841.1:c.2731+256G>A XP_011525143.1:n.2731+256G>A
XM_011526842.1:c.2584+256G>A XP_011525144.1:n.2584+256G>A
XM_011526843.1:c.1900+256G>A XP_011525145.1:n.1900+256G>A
XM_011526844.1:c.1900+256G>A XP_011525146.1:n.1900+256G>A
XM_011526840.2:c.3145+256G>A XP_011525142.1:n.3145+256G>A
XM_011526841.2:c.2731+256G>A XP_011525143.1:n.2731+256G>A
XM_011526844.2:c.1900+256G>A XP_011525146.1:n.1900+256G>A
XM_017026665.1:c.4153+256G>A XP_016882154.1:n.4153+256G>A
NM_001083961.2:c.4153+256G>A MANE Select NP_001077430.1:n.4153+256G>A
NM_173636.5:c.4138+256G>A NP_775907.4:n.4138+256G>A