Canonical Allele Identifier: CA9396061

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36100822T>C , CM000681.2:g.36100822T>C	GRCh38
NC_000019.9:g.36591724T>C , CM000681.1:g.36591724T>C	GRCh37
NC_000019.8:g.41283564T>C	NCBI36
NG_028101.1:g.50942T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.2814T>C	ENSP00000270301.6:p.Ser938=
ENST00000401500.7:c.2814T>C MANE Select	ENSP00000384792.1:p.Ser938=
ENST00000587391.6:c.*1504T>C	ENSP00000465525.1:n.*1504T>C
ENST00000679357.1:c.604T>C
ENST00000679422.1:c.604T>C
ENST00000679682.1:c.2799T>C	ENSP00000506226.1:p.Ser933=
ENST00000679714.1:c.2808T>C	ENSP00000506627.1:p.Ser936=
ENST00000679757.1:c.2463T>C	ENSP00000505158.1:p.Ser821=
ENST00000679858.1:c.*1611T>C	ENSP00000505655.1:n.*1611T>C
ENST00000680211.1:c.-586T>C	ENSP00000506102.1:n.-586T>C
ENST00000680349.1:n.797T>C
ENST00000680403.1:c.2814T>C	ENSP00000505677.1:p.Ser938=
ENST00000680564.1:c.2814T>C	ENSP00000505582.1:p.Ser938=
ENST00000680590.1:c.*1209T>C	ENSP00000505350.1:n.*1209T>C
ENST00000680773.1:n.491T>C
ENST00000680806.1:c.*1643T>C	ENSP00000506418.1:n.*1643T>C
ENST00000681088.1:c.530-392T>C
ENST00000681625.1:c.*146T>C	ENSP00000505555.1:n.*146T>C
ENST00000270301.11:c.2814T>C	ENSP00000270301.6:p.Ser938=
ENST00000401500.6:c.2814T>C	ENSP00000384792.1:p.Ser938=
ENST00000587391.5:c.*1504T>C	ENSP00000465525.1:n.*1504T>C
NM_001083961.1:c.2814T>C	NP_001077430.1:p.Ser938=
NM_173636.4:c.2814T>C	NP_775907.4:p.Ser938=
XM_005258809.2:c.2814T>C	XP_005258866.1:p.Ser938=
XM_011526837.1:c.2799T>C	XP_011525139.1:p.Ser933=
XM_011526838.1:c.2814T>C	XP_011525140.1:p.Ser938=
XM_011526839.1:c.2463T>C	XP_011525141.1:p.Ser821=
XM_011526840.1:c.1806T>C	XP_011525142.1:p.Ser602=
XM_011526841.1:c.1392T>C	XP_011525143.1:p.Ser464=
XM_011526842.1:c.1245T>C	XP_011525144.1:p.Ser415=
XM_011526843.1:c.561T>C	XP_011525145.1:p.Ser187=
XM_011526844.1:c.561T>C	XP_011525146.1:p.Ser187=
XM_011526840.2:c.1806T>C	XP_011525142.1:p.Ser602=
XM_011526841.2:c.1392T>C	XP_011525143.1:p.Ser464=
XM_011526844.2:c.561T>C	XP_011525146.1:p.Ser187=
XM_017026665.1:c.2814T>C	XP_016882154.1:p.Ser938=
NM_001083961.2:c.2814T>C MANE Select	NP_001077430.1:p.Ser938=
NM_173636.5:c.2814T>C	NP_775907.4:p.Ser938=