Canonical Allele Identifier: CA405449968

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102031-G-C
• MyVariant Identifiers: chr19:g.36592933G>C (hg19) ; chr19:g.36102031G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102031G>C , CM000681.2:g.36102031G>C	GRCh38
NC_000019.9:g.36592933G>C , CM000681.1:g.36592933G>C	GRCh37
NC_000019.8:g.41284773G>C	NCBI36
NG_028101.1:g.52151G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3100G>C	ENSP00000270301.6:p.Glu1034Gln
ENST00000401500.7:c.3100G>C MANE Select	ENSP00000384792.1:p.Glu1034Gln
ENST00000587391.6:c.*2375G>C	ENSP00000465525.1:n.*2375G>C
ENST00000679357.1:c.890G>C
ENST00000679422.1:c.779G>C
ENST00000679682.1:c.3085G>C	ENSP00000506226.1:p.Glu1029Gln
ENST00000679714.1:c.3094G>C	ENSP00000506627.1:p.Glu1032Gln
ENST00000679757.1:c.2749G>C	ENSP00000505158.1:p.Glu917Gln
ENST00000679858.1:c.*2482G>C	ENSP00000505655.1:n.*2482G>C
ENST00000680211.1:c.-300G>C	ENSP00000506102.1:n.-300G>C
ENST00000680349.1:n.1083G>C
ENST00000680403.1:c.3100G>C	ENSP00000505677.1:p.Glu1034Gln
ENST00000680564.1:c.2972-706G>C	ENSP00000505582.1:n.2972-706G>C
ENST00000680590.1:c.*1495G>C	ENSP00000505350.1:n.*1495G>C
ENST00000680739.1:c.18G>C
ENST00000680773.1:n.1016G>C
ENST00000680806.1:c.*1818G>C	ENSP00000506418.1:n.*1818G>C
ENST00000680997.1:n.447G>C
ENST00000681088.1:c.762G>C
ENST00000681608.1:n.48G>C
ENST00000681625.1:c.*432G>C	ENSP00000505555.1:n.*432G>C
ENST00000270301.11:c.3100G>C	ENSP00000270301.6:p.Glu1034Gln
ENST00000401500.6:c.3100G>C	ENSP00000384792.1:p.Glu1034Gln
ENST00000587391.5:c.*2375G>C	ENSP00000465525.1:n.*2375G>C
NM_001083961.1:c.3100G>C	NP_001077430.1:p.Glu1034Gln
NM_173636.4:c.3100G>C	NP_775907.4:p.Glu1034Gln
XM_005258809.2:c.2989G>C	XP_005258866.1:p.Glu997Gln
XM_011526837.1:c.3085G>C	XP_011525139.1:p.Glu1029Gln
XM_011526838.1:c.2972-706G>C	XP_011525140.1:n.2972-706G>C
XM_011526839.1:c.2749G>C	XP_011525141.1:p.Glu917Gln
XM_011526840.1:c.2092G>C	XP_011525142.1:p.Glu698Gln
XM_011526841.1:c.1678G>C	XP_011525143.1:p.Glu560Gln
XM_011526842.1:c.1531G>C	XP_011525144.1:p.Glu511Gln
XM_011526843.1:c.847G>C	XP_011525145.1:p.Glu283Gln
XM_011526844.1:c.847G>C	XP_011525146.1:p.Glu283Gln
XM_011526840.2:c.2092G>C	XP_011525142.1:p.Glu698Gln
XM_011526841.2:c.1678G>C	XP_011525143.1:p.Glu560Gln
XM_011526844.2:c.847G>C	XP_011525146.1:p.Glu283Gln
XM_017026665.1:c.3100G>C	XP_016882154.1:p.Glu1034Gln
NM_001083961.2:c.3100G>C MANE Select	NP_001077430.1:p.Glu1034Gln
NM_173636.5:c.3100G>C	NP_775907.4:p.Glu1034Gln