Canonical Allele Identifier: CA2333972128
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104417T= , CM000681.2:g.36104417T= GRCh38
NC_000019.9:g.36595319T= , CM000681.1:g.36595319T= GRCh37
NC_000019.8:g.41287159T= NCBI36
NG_028101.1:g.54537T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4139-101T= ENSP00000270301.6:n.4139-101T=
ENST00000401500.7:c.4154-101T= MANE Select ENSP00000384792.1:n.4154-101T=
ENST00000587391.6:c.*4014-101T= ENSP00000465525.1:n.*4014-101T=
ENST00000679357.1:c.2234-101T=
ENST00000679598.1:c.919-121T=
ENST00000679682.1:c.4139-101T= ENSP00000506226.1:n.4139-101T=
ENST00000679714.1:c.4148-101T= ENSP00000506627.1:n.4148-101T=
ENST00000679757.1:c.3803-101T= ENSP00000505158.1:n.3803-101T=
ENST00000679858.1:c.*3536-101T= ENSP00000505655.1:n.*3536-101T=
ENST00000680211.1:c.755-101T= ENSP00000506102.1:n.755-101T=
ENST00000680280.1:n.1657-101T=
ENST00000680349.1:n.2803-101T=
ENST00000680403.1:c.4139-101T= ENSP00000505677.1:n.4139-101T=
ENST00000680564.1:c.3905-101T= ENSP00000505582.1:n.3905-101T=
ENST00000680590.1:c.*2534-101T= ENSP00000505350.1:n.*2534-101T=
ENST00000680597.1:c.887-101T=
ENST00000680739.1:c.1169-101T=
ENST00000680773.1:n.2655-101T=
ENST00000680806.1:c.*3457-101T= ENSP00000506418.1:n.*3457-101T=
ENST00000680997.1:n.2086-101T=
ENST00000681608.1:n.1999-101T=
ENST00000681625.1:c.*1486-101T= ENSP00000505555.1:n.*1486-101T=
ENST00000681648.1:n.2104T=
ENST00000270301.11:c.4139-101T= ENSP00000270301.6:n.4139-101T=
ENST00000401500.6:c.4154-101T= ENSP00000384792.1:n.4154-101T=
ENST00000587391.5:c.*4014-101T= ENSP00000465525.1:n.*4014-101T=
NM_001083961.1:c.4154-101T= NP_001077430.1:n.4154-101T=
NM_173636.4:c.4139-101T= NP_775907.4:n.4139-101T=
XM_005258809.2:c.4043-101T= XP_005258866.1:n.4043-101T=
XM_011526837.1:c.4139-101T= XP_011525139.1:n.4139-101T=
XM_011526838.1:c.3905-101T= XP_011525140.1:n.3905-101T=
XM_011526839.1:c.3803-101T= XP_011525141.1:n.3803-101T=
XM_011526840.1:c.3146-101T= XP_011525142.1:n.3146-101T=
XM_011526841.1:c.2732-101T= XP_011525143.1:n.2732-101T=
XM_011526842.1:c.2585-101T= XP_011525144.1:n.2585-101T=
XM_011526843.1:c.1901-101T= XP_011525145.1:n.1901-101T=
XM_011526844.1:c.1901-101T= XP_011525146.1:n.1901-101T=
XM_011526840.2:c.3146-101T= XP_011525142.1:n.3146-101T=
XM_011526841.2:c.2732-101T= XP_011525143.1:n.2732-101T=
XM_011526844.2:c.1901-101T= XP_011525146.1:n.1901-101T=
XM_017026665.1:c.4154-101T= XP_016882154.1:n.4154-101T=
NM_001083961.2:c.4154-101T= MANE Select NP_001077430.1:n.4154-101T=
NM_173636.5:c.4139-101T= NP_775907.4:n.4139-101T=