Canonical Allele Identifier: CA405451601

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593670G>C (hg19) ; chr19:g.36102768G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102768G>C , CM000681.2:g.36102768G>C	GRCh38
NC_000019.9:g.36593670G>C , CM000681.1:g.36593670G>C	GRCh37
NC_000019.8:g.41285510G>C	NCBI36
NG_028101.1:g.52888G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3237G>C	ENSP00000270301.6:p.Glu1079Asp
ENST00000401500.7:c.3252G>C MANE Select	ENSP00000384792.1:p.Glu1084Asp
ENST00000587391.6:c.*3112G>C	ENSP00000465525.1:n.*3112G>C
ENST00000679357.1:c.1332G>C
ENST00000679598.1:c.17G>C
ENST00000679682.1:c.3237G>C	ENSP00000506226.1:p.Glu1079Asp
ENST00000679714.1:c.3246G>C	ENSP00000506627.1:p.Glu1082Asp
ENST00000679757.1:c.2901G>C	ENSP00000505158.1:p.Glu967Asp
ENST00000679858.1:c.*2634G>C	ENSP00000505655.1:n.*2634G>C
ENST00000680211.1:c.-148G>C	ENSP00000506102.1:n.-148G>C
ENST00000680280.1:n.539G>C
ENST00000680349.1:n.1820G>C
ENST00000680403.1:c.3237G>C	ENSP00000505677.1:p.Glu1079Asp
ENST00000680564.1:c.3003G>C	ENSP00000505582.1:p.Glu1001Asp
ENST00000680590.1:c.*1632G>C	ENSP00000505350.1:n.*1632G>C
ENST00000680597.1:c.17G>C
ENST00000680739.1:c.267G>C
ENST00000680773.1:n.1753G>C
ENST00000680806.1:c.*2555G>C	ENSP00000506418.1:n.*2555G>C
ENST00000680997.1:n.1184G>C
ENST00000681608.1:n.785G>C
ENST00000681625.1:c.*584G>C	ENSP00000505555.1:n.*584G>C
ENST00000681648.1:n.551G>C
ENST00000270301.11:c.3237G>C	ENSP00000270301.6:p.Glu1079Asp
ENST00000401500.6:c.3252G>C	ENSP00000384792.1:p.Glu1084Asp
ENST00000587391.5:c.*3112G>C	ENSP00000465525.1:n.*3112G>C
NM_001083961.1:c.3252G>C	NP_001077430.1:p.Glu1084Asp
NM_173636.4:c.3237G>C	NP_775907.4:p.Glu1079Asp
XM_005258809.2:c.3141G>C	XP_005258866.1:p.Glu1047Asp
XM_011526837.1:c.3237G>C	XP_011525139.1:p.Glu1079Asp
XM_011526838.1:c.3003G>C	XP_011525140.1:p.Glu1001Asp
XM_011526839.1:c.2901G>C	XP_011525141.1:p.Glu967Asp
XM_011526840.1:c.2244G>C	XP_011525142.1:p.Glu748Asp
XM_011526841.1:c.1830G>C	XP_011525143.1:p.Glu610Asp
XM_011526842.1:c.1683G>C	XP_011525144.1:p.Glu561Asp
XM_011526843.1:c.999G>C	XP_011525145.1:p.Glu333Asp
XM_011526844.1:c.999G>C	XP_011525146.1:p.Glu333Asp
XM_011526840.2:c.2244G>C	XP_011525142.1:p.Glu748Asp
XM_011526841.2:c.1830G>C	XP_011525143.1:p.Glu610Asp
XM_011526844.2:c.999G>C	XP_011525146.1:p.Glu333Asp
XM_017026665.1:c.3252G>C	XP_016882154.1:p.Glu1084Asp
NM_001083961.2:c.3252G>C MANE Select	NP_001077430.1:p.Glu1084Asp
NM_173636.5:c.3237G>C	NP_775907.4:p.Glu1079Asp