Canonical Allele Identifier: CA405449984

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592935A>C (hg19) ; chr19:g.36102033A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102033A>C , CM000681.2:g.36102033A>C	GRCh38
NC_000019.9:g.36592935A>C , CM000681.1:g.36592935A>C	GRCh37
NC_000019.8:g.41284775A>C	NCBI36
NG_028101.1:g.52153A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3102A>C	ENSP00000270301.6:p.Glu1034Asp
ENST00000401500.7:c.3102A>C MANE Select	ENSP00000384792.1:p.Glu1034Asp
ENST00000587391.6:c.*2377A>C	ENSP00000465525.1:n.*2377A>C
ENST00000679357.1:c.892A>C
ENST00000679422.1:c.781A>C
ENST00000679682.1:c.3087A>C	ENSP00000506226.1:p.Glu1029Asp
ENST00000679714.1:c.3096A>C	ENSP00000506627.1:p.Glu1032Asp
ENST00000679757.1:c.2751A>C	ENSP00000505158.1:p.Glu917Asp
ENST00000679858.1:c.*2484A>C	ENSP00000505655.1:n.*2484A>C
ENST00000680211.1:c.-298A>C	ENSP00000506102.1:n.-298A>C
ENST00000680349.1:n.1085A>C
ENST00000680403.1:c.3102A>C	ENSP00000505677.1:p.Glu1034Asp
ENST00000680564.1:c.2972-704A>C	ENSP00000505582.1:n.2972-704A>C
ENST00000680590.1:c.*1497A>C	ENSP00000505350.1:n.*1497A>C
ENST00000680739.1:c.20A>C
ENST00000680773.1:n.1018A>C
ENST00000680806.1:c.*1820A>C	ENSP00000506418.1:n.*1820A>C
ENST00000680997.1:n.449A>C
ENST00000681088.1:c.764A>C
ENST00000681608.1:n.50A>C
ENST00000681625.1:c.*434A>C	ENSP00000505555.1:n.*434A>C
ENST00000270301.11:c.3102A>C	ENSP00000270301.6:p.Glu1034Asp
ENST00000401500.6:c.3102A>C	ENSP00000384792.1:p.Glu1034Asp
ENST00000587391.5:c.*2377A>C	ENSP00000465525.1:n.*2377A>C
NM_001083961.1:c.3102A>C	NP_001077430.1:p.Glu1034Asp
NM_173636.4:c.3102A>C	NP_775907.4:p.Glu1034Asp
XM_005258809.2:c.2991A>C	XP_005258866.1:p.Glu997Asp
XM_011526837.1:c.3087A>C	XP_011525139.1:p.Glu1029Asp
XM_011526838.1:c.2972-704A>C	XP_011525140.1:n.2972-704A>C
XM_011526839.1:c.2751A>C	XP_011525141.1:p.Glu917Asp
XM_011526840.1:c.2094A>C	XP_011525142.1:p.Glu698Asp
XM_011526841.1:c.1680A>C	XP_011525143.1:p.Glu560Asp
XM_011526842.1:c.1533A>C	XP_011525144.1:p.Glu511Asp
XM_011526843.1:c.849A>C	XP_011525145.1:p.Glu283Asp
XM_011526844.1:c.849A>C	XP_011525146.1:p.Glu283Asp
XM_011526840.2:c.2094A>C	XP_011525142.1:p.Glu698Asp
XM_011526841.2:c.1680A>C	XP_011525143.1:p.Glu560Asp
XM_011526844.2:c.849A>C	XP_011525146.1:p.Glu283Asp
XM_017026665.1:c.3102A>C	XP_016882154.1:p.Glu1034Asp
NM_001083961.2:c.3102A>C MANE Select	NP_001077430.1:p.Glu1034Asp
NM_173636.5:c.3102A>C	NP_775907.4:p.Glu1034Asp