Canonical Allele Identifier: CA405426336
Gene: WDR62 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36065990A>G , CM000681.2:g.36065990A>G GRCh38
NC_000019.9:g.36556892A>G , CM000681.1:g.36556892A>G GRCh37
NC_000019.8:g.41248732A>G NCBI36
NG_028101.1:g.16110A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.365A>G ENSP00000270301.6:p.Asp122Gly
ENST00000401500.7:c.365A>G MANE Select ENSP00000384792.1:p.Asp122Gly
ENST00000427823.3:c.449A>G ENSP00000413475.4:p.Asp150Gly
ENST00000587391.6:c.365A>G ENSP00000465525.1:p.Asp122Gly
ENST00000589953.2:n.429A>G
ENST00000644764.2:c.365A>G ENSP00000494253.2:p.Asp122Gly
ENST00000679682.1:c.365A>G ENSP00000506226.1:p.Asp122Gly
ENST00000679714.1:c.365A>G ENSP00000506627.1:p.Asp122Gly
ENST00000679757.1:c.365A>G ENSP00000505158.1:p.Asp122Gly
ENST00000679858.1:c.365A>G ENSP00000505655.1:p.Asp122Gly
ENST00000680321.1:c.365A>G ENSP00000505525.1:p.Asp122Gly
ENST00000680359.1:c.365A>G ENSP00000506079.1:p.Asp122Gly
ENST00000680403.1:c.365A>G ENSP00000505677.1:p.Asp122Gly
ENST00000680489.1:n.688A>G
ENST00000680564.1:c.365A>G ENSP00000505582.1:p.Asp122Gly
ENST00000680590.1:c.365A>G ENSP00000505350.1:p.Asp122Gly
ENST00000680806.1:c.365A>G ENSP00000506418.1:p.Asp122Gly
ENST00000681542.1:c.365A>G ENSP00000505251.1:p.Asp122Gly
ENST00000681625.1:c.365A>G ENSP00000505555.1:p.Asp122Gly
ENST00000681809.1:c.365A>G ENSP00000505740.1:p.Asp122Gly
ENST00000270301.11:c.365A>G ENSP00000270301.6:p.Asp122Gly
ENST00000378860.8:n.456A>G
ENST00000401500.6:c.365A>G ENSP00000384792.1:p.Asp122Gly
ENST00000427823.2:c.431A>G ENSP00000413475.3:p.Asp144Gly
ENST00000587391.5:c.365A>G ENSP00000465525.1:p.Asp122Gly
NM_001083961.1:c.365A>G NP_001077430.1:p.Asp122Gly
NM_173636.4:c.365A>G NP_775907.4:p.Asp122Gly
XM_005258809.2:c.365A>G XP_005258866.1:p.Asp122Gly
XM_011526837.1:c.365A>G XP_011525139.1:p.Asp122Gly
XM_011526838.1:c.365A>G XP_011525140.1:p.Asp122Gly
XM_011526839.1:c.365A>G XP_011525141.1:p.Asp122Gly
XM_017026665.1:c.365A>G XP_016882154.1:p.Asp122Gly
XR_001753671.1:n.456A>G
XR_001753672.1:n.456A>G
NM_001083961.2:c.365A>G MANE Select NP_001077430.1:p.Asp122Gly
NM_173636.5:c.365A>G NP_775907.4:p.Asp122Gly