Canonical Allele Identifier: CA2333970944

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102113G= , CM000681.2:g.36102113G=	GRCh38
NC_000019.9:g.36593015G= , CM000681.1:g.36593015G=	GRCh37
NC_000019.8:g.41284855G=	NCBI36
NG_028101.1:g.52233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3182G=	ENSP00000270301.6:p.Arg1061=
ENST00000401500.7:c.3182G= MANE Select	ENSP00000384792.1:p.Arg1061=
ENST00000587391.6:c.*2457G=	ENSP00000465525.1:n.*2457G=
ENST00000679357.1:c.972G=
ENST00000679422.1:c.861G=
ENST00000679682.1:c.3167G=	ENSP00000506226.1:p.Arg1056=
ENST00000679714.1:c.3176G=	ENSP00000506627.1:p.Arg1059=
ENST00000679757.1:c.2831G=	ENSP00000505158.1:p.Arg944=
ENST00000679858.1:c.*2564G=	ENSP00000505655.1:n.*2564G=
ENST00000680211.1:c.-218G=	ENSP00000506102.1:n.-218G=
ENST00000680349.1:n.1165G=
ENST00000680403.1:c.3182G=	ENSP00000505677.1:p.Arg1061=
ENST00000680564.1:c.2972-624G=	ENSP00000505582.1:n.2972-624G=
ENST00000680590.1:c.*1577G=	ENSP00000505350.1:n.*1577G=
ENST00000680739.1:c.100G=
ENST00000680773.1:n.1098G=
ENST00000680806.1:c.*1900G=	ENSP00000506418.1:n.*1900G=
ENST00000680997.1:n.529G=
ENST00000681088.1:c.844G=
ENST00000681608.1:n.130G=
ENST00000681625.1:c.*514G=	ENSP00000505555.1:n.*514G=
ENST00000270301.11:c.3182G=	ENSP00000270301.6:p.Arg1061=
ENST00000401500.6:c.3182G=	ENSP00000384792.1:p.Arg1061=
ENST00000587391.5:c.*2457G=	ENSP00000465525.1:n.*2457G=
NM_001083961.1:c.3182G=	NP_001077430.1:p.Arg1061=
NM_173636.4:c.3182G=	NP_775907.4:p.Arg1061=
XM_005258809.2:c.3071G=	XP_005258866.1:p.Arg1024=
XM_011526837.1:c.3167G=	XP_011525139.1:p.Arg1056=
XM_011526838.1:c.2972-624G=	XP_011525140.1:n.2972-624G=
XM_011526839.1:c.2831G=	XP_011525141.1:p.Arg944=
XM_011526840.1:c.2174G=	XP_011525142.1:p.Arg725=
XM_011526841.1:c.1760G=	XP_011525143.1:p.Arg587=
XM_011526842.1:c.1613G=	XP_011525144.1:p.Arg538=
XM_011526843.1:c.929G=	XP_011525145.1:p.Arg310=
XM_011526844.1:c.929G=	XP_011525146.1:p.Arg310=
XM_011526840.2:c.2174G=	XP_011525142.1:p.Arg725=
XM_011526841.2:c.1760G=	XP_011525143.1:p.Arg587=
XM_011526844.2:c.929G=	XP_011525146.1:p.Arg310=
XM_017026665.1:c.3182G=	XP_016882154.1:p.Arg1061=
NM_001083961.2:c.3182G= MANE Select	NP_001077430.1:p.Arg1061=
NM_173636.5:c.3182G=	NP_775907.4:p.Arg1061=