Canonical Allele Identifier: CA405460548

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595467T>G (hg19) ; chr19:g.36104565T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104565T>G , CM000681.2:g.36104565T>G	GRCh38
NC_000019.9:g.36595467T>G , CM000681.1:g.36595467T>G	GRCh37
NC_000019.8:g.41287307T>G	NCBI36
NG_028101.1:g.54685T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4186T>G	ENSP00000270301.6:p.Trp1396Gly
ENST00000401500.7:c.4201T>G MANE Select	ENSP00000384792.1:p.Trp1401Gly
ENST00000587391.6:c.*4061T>G	ENSP00000465525.1:n.*4061T>G
ENST00000679357.1:c.2281T>G
ENST00000679598.1:c.946T>G
ENST00000679682.1:c.4186T>G	ENSP00000506226.1:p.Trp1396Gly
ENST00000679714.1:c.4195T>G	ENSP00000506627.1:p.Trp1399Gly
ENST00000679757.1:c.3850T>G	ENSP00000505158.1:p.Trp1284Gly
ENST00000679858.1:c.*3583T>G	ENSP00000505655.1:n.*3583T>G
ENST00000680211.1:c.802T>G	ENSP00000506102.1:p.Trp268Gly
ENST00000680280.1:n.1704T>G
ENST00000680349.1:n.2850T>G
ENST00000680403.1:c.4186T>G	ENSP00000505677.1:p.Trp1396Gly
ENST00000680564.1:c.3952T>G	ENSP00000505582.1:p.Trp1318Gly
ENST00000680590.1:c.*2581T>G	ENSP00000505350.1:n.*2581T>G
ENST00000680597.1:c.934T>G
ENST00000680739.1:c.1216T>G
ENST00000680773.1:n.2702T>G
ENST00000680806.1:c.*3504T>G	ENSP00000506418.1:n.*3504T>G
ENST00000680997.1:n.2133T>G
ENST00000681608.1:n.2046T>G
ENST00000681625.1:c.*1533T>G	ENSP00000505555.1:n.*1533T>G
ENST00000681648.1:n.2252T>G
ENST00000270301.11:c.4186T>G	ENSP00000270301.6:p.Trp1396Gly
ENST00000401500.6:c.4201T>G	ENSP00000384792.1:p.Trp1401Gly
ENST00000587391.5:c.*4061T>G	ENSP00000465525.1:n.*4061T>G
NM_001083961.1:c.4201T>G	NP_001077430.1:p.Trp1401Gly
NM_173636.4:c.4186T>G	NP_775907.4:p.Trp1396Gly
XM_005258809.2:c.4090T>G	XP_005258866.1:p.Trp1364Gly
XM_011526837.1:c.4186T>G	XP_011525139.1:p.Trp1396Gly
XM_011526838.1:c.3952T>G	XP_011525140.1:p.Trp1318Gly
XM_011526839.1:c.3850T>G	XP_011525141.1:p.Trp1284Gly
XM_011526840.1:c.3193T>G	XP_011525142.1:p.Trp1065Gly
XM_011526841.1:c.2779T>G	XP_011525143.1:p.Trp927Gly
XM_011526842.1:c.2632T>G	XP_011525144.1:p.Trp878Gly
XM_011526843.1:c.1948T>G	XP_011525145.1:p.Trp650Gly
XM_011526844.1:c.1948T>G	XP_011525146.1:p.Trp650Gly
XM_011526840.2:c.3193T>G	XP_011525142.1:p.Trp1065Gly
XM_011526841.2:c.2779T>G	XP_011525143.1:p.Trp927Gly
XM_011526844.2:c.1948T>G	XP_011525146.1:p.Trp650Gly
XM_017026665.1:c.4201T>G	XP_016882154.1:p.Trp1401Gly
NM_001083961.2:c.4201T>G MANE Select	NP_001077430.1:p.Trp1401Gly
NM_173636.5:c.4186T>G	NP_775907.4:p.Trp1396Gly