Canonical Allele Identifier: CA2333970913

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102051C= , CM000681.2:g.36102051C=	GRCh38
NC_000019.9:g.36592953C= , CM000681.1:g.36592953C=	GRCh37
NC_000019.8:g.41284793C=	NCBI36
NG_028101.1:g.52171C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3120C=	ENSP00000270301.6:p.Pro1040=
ENST00000401500.7:c.3120C= MANE Select	ENSP00000384792.1:p.Pro1040=
ENST00000587391.6:c.*2395C=	ENSP00000465525.1:n.*2395C=
ENST00000679357.1:c.910C=
ENST00000679422.1:c.799C=
ENST00000679682.1:c.3105C=	ENSP00000506226.1:p.Pro1035=
ENST00000679714.1:c.3114C=	ENSP00000506627.1:p.Pro1038=
ENST00000679757.1:c.2769C=	ENSP00000505158.1:p.Pro923=
ENST00000679858.1:c.*2502C=	ENSP00000505655.1:n.*2502C=
ENST00000680211.1:c.-280C=	ENSP00000506102.1:n.-280C=
ENST00000680349.1:n.1103C=
ENST00000680403.1:c.3120C=	ENSP00000505677.1:p.Pro1040=
ENST00000680564.1:c.2972-686C=	ENSP00000505582.1:n.2972-686C=
ENST00000680590.1:c.*1515C=	ENSP00000505350.1:n.*1515C=
ENST00000680739.1:c.38C=
ENST00000680773.1:n.1036C=
ENST00000680806.1:c.*1838C=	ENSP00000506418.1:n.*1838C=
ENST00000680997.1:n.467C=
ENST00000681088.1:c.782C=
ENST00000681608.1:n.68C=
ENST00000681625.1:c.*452C=	ENSP00000505555.1:n.*452C=
ENST00000270301.11:c.3120C=	ENSP00000270301.6:p.Pro1040=
ENST00000401500.6:c.3120C=	ENSP00000384792.1:p.Pro1040=
ENST00000587391.5:c.*2395C=	ENSP00000465525.1:n.*2395C=
NM_001083961.1:c.3120C=	NP_001077430.1:p.Pro1040=
NM_173636.4:c.3120C=	NP_775907.4:p.Pro1040=
XM_005258809.2:c.3009C=	XP_005258866.1:p.Pro1003=
XM_011526837.1:c.3105C=	XP_011525139.1:p.Pro1035=
XM_011526838.1:c.2972-686C=	XP_011525140.1:n.2972-686C=
XM_011526839.1:c.2769C=	XP_011525141.1:p.Pro923=
XM_011526840.1:c.2112C=	XP_011525142.1:p.Pro704=
XM_011526841.1:c.1698C=	XP_011525143.1:p.Pro566=
XM_011526842.1:c.1551C=	XP_011525144.1:p.Pro517=
XM_011526843.1:c.867C=	XP_011525145.1:p.Pro289=
XM_011526844.1:c.867C=	XP_011525146.1:p.Pro289=
XM_011526840.2:c.2112C=	XP_011525142.1:p.Pro704=
XM_011526841.2:c.1698C=	XP_011525143.1:p.Pro566=
XM_011526844.2:c.867C=	XP_011525146.1:p.Pro289=
XM_017026665.1:c.3120C=	XP_016882154.1:p.Pro1040=
NM_001083961.2:c.3120C= MANE Select	NP_001077430.1:p.Pro1040=
NM_173636.5:c.3120C=	NP_775907.4:p.Pro1040=