Canonical Allele Identifier: CA405450828

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593038G>C (hg19) ; chr19:g.36102136G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102136G>C , CM000681.2:g.36102136G>C	GRCh38
NC_000019.9:g.36593038G>C , CM000681.1:g.36593038G>C	GRCh37
NC_000019.8:g.41284878G>C	NCBI36
NG_028101.1:g.52256G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3205G>C	ENSP00000270301.6:p.Glu1069Gln
ENST00000401500.7:c.3205G>C MANE Select	ENSP00000384792.1:p.Glu1069Gln
ENST00000587391.6:c.*2480G>C	ENSP00000465525.1:n.*2480G>C
ENST00000679357.1:c.995G>C
ENST00000679422.1:c.884G>C
ENST00000679682.1:c.3190G>C	ENSP00000506226.1:p.Glu1064Gln
ENST00000679714.1:c.3199G>C	ENSP00000506627.1:p.Glu1067Gln
ENST00000679757.1:c.2854G>C	ENSP00000505158.1:p.Glu952Gln
ENST00000679858.1:c.*2587G>C	ENSP00000505655.1:n.*2587G>C
ENST00000680211.1:c.-195G>C	ENSP00000506102.1:n.-195G>C
ENST00000680349.1:n.1188G>C
ENST00000680403.1:c.3205G>C	ENSP00000505677.1:p.Glu1069Gln
ENST00000680564.1:c.2972-601G>C	ENSP00000505582.1:n.2972-601G>C
ENST00000680590.1:c.*1600G>C	ENSP00000505350.1:n.*1600G>C
ENST00000680739.1:c.123G>C
ENST00000680773.1:n.1121G>C
ENST00000680806.1:c.*1923G>C	ENSP00000506418.1:n.*1923G>C
ENST00000680997.1:n.552G>C
ENST00000681088.1:c.867G>C
ENST00000681608.1:n.153G>C
ENST00000681625.1:c.*537G>C	ENSP00000505555.1:n.*537G>C
ENST00000270301.11:c.3205G>C	ENSP00000270301.6:p.Glu1069Gln
ENST00000401500.6:c.3205G>C	ENSP00000384792.1:p.Glu1069Gln
ENST00000587391.5:c.*2480G>C	ENSP00000465525.1:n.*2480G>C
NM_001083961.1:c.3205G>C	NP_001077430.1:p.Glu1069Gln
NM_173636.4:c.3205G>C	NP_775907.4:p.Glu1069Gln
XM_005258809.2:c.3094G>C	XP_005258866.1:p.Glu1032Gln
XM_011526837.1:c.3190G>C	XP_011525139.1:p.Glu1064Gln
XM_011526838.1:c.2972-601G>C	XP_011525140.1:n.2972-601G>C
XM_011526839.1:c.2854G>C	XP_011525141.1:p.Glu952Gln
XM_011526840.1:c.2197G>C	XP_011525142.1:p.Glu733Gln
XM_011526841.1:c.1783G>C	XP_011525143.1:p.Glu595Gln
XM_011526842.1:c.1636G>C	XP_011525144.1:p.Glu546Gln
XM_011526843.1:c.952G>C	XP_011525145.1:p.Glu318Gln
XM_011526844.1:c.952G>C	XP_011525146.1:p.Glu318Gln
XM_011526840.2:c.2197G>C	XP_011525142.1:p.Glu733Gln
XM_011526841.2:c.1783G>C	XP_011525143.1:p.Glu595Gln
XM_011526844.2:c.952G>C	XP_011525146.1:p.Glu318Gln
XM_017026665.1:c.3205G>C	XP_016882154.1:p.Glu1069Gln
NM_001083961.2:c.3205G>C MANE Select	NP_001077430.1:p.Glu1069Gln
NM_173636.5:c.3205G>C	NP_775907.4:p.Glu1069Gln