Canonical Allele Identifier: CA2333972210

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104600T= , CM000681.2:g.36104600T=	GRCh38
NC_000019.9:g.36595502T= , CM000681.1:g.36595502T=	GRCh37
NC_000019.8:g.41287342T=	NCBI36
NG_028101.1:g.54720T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4221T=	ENSP00000270301.6:p.Leu1407=
ENST00000401500.7:c.4236T= MANE Select	ENSP00000384792.1:p.Leu1412=
ENST00000587391.6:c.*4096T=	ENSP00000465525.1:n.*4096T=
ENST00000679357.1:c.2316T=
ENST00000679598.1:c.981T=
ENST00000679682.1:c.4221T=	ENSP00000506226.1:p.Leu1407=
ENST00000679714.1:c.4230T=	ENSP00000506627.1:p.Leu1410=
ENST00000679757.1:c.3885T=	ENSP00000505158.1:p.Leu1295=
ENST00000679858.1:c.*3618T=	ENSP00000505655.1:n.*3618T=
ENST00000680211.1:c.837T=	ENSP00000506102.1:p.Leu279=
ENST00000680280.1:n.1739T=
ENST00000680349.1:n.2885T=
ENST00000680403.1:c.4221T=	ENSP00000505677.1:p.Leu1407=
ENST00000680564.1:c.3987T=	ENSP00000505582.1:p.Leu1329=
ENST00000680590.1:c.*2616T=	ENSP00000505350.1:n.*2616T=
ENST00000680597.1:c.969T=
ENST00000680739.1:c.1251T=
ENST00000680773.1:n.2737T=
ENST00000680806.1:c.*3539T=	ENSP00000506418.1:n.*3539T=
ENST00000680997.1:n.2168T=
ENST00000681608.1:n.2081T=
ENST00000681625.1:c.*1568T=	ENSP00000505555.1:n.*1568T=
ENST00000681648.1:n.2287T=
ENST00000270301.11:c.4221T=	ENSP00000270301.6:p.Leu1407=
ENST00000401500.6:c.4236T=	ENSP00000384792.1:p.Leu1412=
ENST00000587391.5:c.*4096T=	ENSP00000465525.1:n.*4096T=
NM_001083961.1:c.4236T=	NP_001077430.1:p.Leu1412=
NM_173636.4:c.4221T=	NP_775907.4:p.Leu1407=
XM_005258809.2:c.4125T=	XP_005258866.1:p.Leu1375=
XM_011526837.1:c.4221T=	XP_011525139.1:p.Leu1407=
XM_011526838.1:c.3987T=	XP_011525140.1:p.Leu1329=
XM_011526839.1:c.3885T=	XP_011525141.1:p.Leu1295=
XM_011526840.1:c.3228T=	XP_011525142.1:p.Leu1076=
XM_011526841.1:c.2814T=	XP_011525143.1:p.Leu938=
XM_011526842.1:c.2667T=	XP_011525144.1:p.Leu889=
XM_011526843.1:c.1983T=	XP_011525145.1:p.Leu661=
XM_011526844.1:c.1983T=	XP_011525146.1:p.Leu661=
XM_011526840.2:c.3228T=	XP_011525142.1:p.Leu1076=
XM_011526841.2:c.2814T=	XP_011525143.1:p.Leu938=
XM_011526844.2:c.1983T=	XP_011525146.1:p.Leu661=
XM_017026665.1:c.4236T=	XP_016882154.1:p.Leu1412=
NM_001083961.2:c.4236T= MANE Select	NP_001077430.1:p.Leu1412=
NM_173636.5:c.4221T=	NP_775907.4:p.Leu1407=