Canonical Allele Identifier: CA10603443
Gene: WDR62 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36094166T>G , CM000681.2:g.36094166T>G GRCh38
NC_000019.9:g.36585068T>G , CM000681.1:g.36585068T>G GRCh37
NC_000019.8:g.41276908T>G NCBI36
NG_028101.1:g.44286T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.2467+2T>G ENSP00000270301.6:n.2467+2T>G
ENST00000401500.7:c.2467+2T>G MANE Select ENSP00000384792.1:n.2467+2T>G
ENST00000587391.6:c.*1157+2T>G ENSP00000465525.1:n.*1157+2T>G
ENST00000679357.1:c.257+2T>G
ENST00000679422.1:c.257+2T>G
ENST00000679682.1:c.2452+2T>G ENSP00000506226.1:n.2452+2T>G
ENST00000679714.1:c.2461+2T>G ENSP00000506627.1:n.2461+2T>G
ENST00000679757.1:c.2116+2T>G ENSP00000505158.1:n.2116+2T>G
ENST00000679858.1:c.*1264+2T>G ENSP00000505655.1:n.*1264+2T>G
ENST00000680349.1:n.450+2T>G
ENST00000680377.1:c.741+2T>G
ENST00000680403.1:c.2467+2T>G ENSP00000505677.1:n.2467+2T>G
ENST00000680564.1:c.2467+2T>G ENSP00000505582.1:n.2467+2T>G
ENST00000680590.1:c.*866+2T>G ENSP00000505350.1:n.*866+2T>G
ENST00000680806.1:c.*1296+2T>G ENSP00000506418.1:n.*1296+2T>G
ENST00000680858.1:c.665+2T>G
ENST00000681088.1:c.257+2T>G
ENST00000681302.1:c.853+2T>G
ENST00000681625.1:c.2452+2T>G ENSP00000505555.1:n.2452+2T>G
ENST00000270301.11:c.2467+2T>G ENSP00000270301.6:n.2467+2T>G
ENST00000401500.6:c.2467+2T>G ENSP00000384792.1:n.2467+2T>G
ENST00000587391.5:c.*1157+2T>G ENSP00000465525.1:n.*1157+2T>G
NM_001083961.1:c.2467+2T>G NP_001077430.1:n.2467+2T>G
NM_173636.4:c.2467+2T>G NP_775907.4:n.2467+2T>G
XM_005258809.2:c.2467+2T>G XP_005258866.1:n.2467+2T>G
XM_011526837.1:c.2452+2T>G XP_011525139.1:n.2452+2T>G
XM_011526838.1:c.2467+2T>G XP_011525140.1:n.2467+2T>G
XM_011526839.1:c.2116+2T>G XP_011525141.1:n.2116+2T>G
XM_011526840.1:c.1459+2T>G XP_011525142.1:n.1459+2T>G
XM_011526841.1:c.1045+2T>G XP_011525143.1:n.1045+2T>G
XM_011526842.1:c.898+2T>G XP_011525144.1:n.898+2T>G
XM_011526843.1:c.214+2T>G XP_011525145.1:n.214+2T>G
XM_011526844.1:c.214+2T>G XP_011525146.1:n.214+2T>G
XM_011526840.2:c.1459+2T>G XP_011525142.1:n.1459+2T>G
XM_011526841.2:c.1045+2T>G XP_011525143.1:n.1045+2T>G
XM_011526844.2:c.214+2T>G XP_011525146.1:n.214+2T>G
XM_017026665.1:c.2467+2T>G XP_016882154.1:n.2467+2T>G
NM_001083961.2:c.2467+2T>G MANE Select NP_001077430.1:n.2467+2T>G
NM_173636.5:c.2467+2T>G NP_775907.4:n.2467+2T>G
Search 100 bp 5'
Search 100 bp 3'