Canonical Allele Identifier: CA405460657

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595479G>C (hg19) ; chr19:g.36104577G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104577G>C , CM000681.2:g.36104577G>C	GRCh38
NC_000019.9:g.36595479G>C , CM000681.1:g.36595479G>C	GRCh37
NC_000019.8:g.41287319G>C	NCBI36
NG_028101.1:g.54697G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4198G>C	ENSP00000270301.6:p.Glu1400Gln
ENST00000401500.7:c.4213G>C MANE Select	ENSP00000384792.1:p.Glu1405Gln
ENST00000587391.6:c.*4073G>C	ENSP00000465525.1:n.*4073G>C
ENST00000679357.1:c.2293G>C
ENST00000679598.1:c.958G>C
ENST00000679682.1:c.4198G>C	ENSP00000506226.1:p.Glu1400Gln
ENST00000679714.1:c.4207G>C	ENSP00000506627.1:p.Glu1403Gln
ENST00000679757.1:c.3862G>C	ENSP00000505158.1:p.Glu1288Gln
ENST00000679858.1:c.*3595G>C	ENSP00000505655.1:n.*3595G>C
ENST00000680211.1:c.814G>C	ENSP00000506102.1:p.Glu272Gln
ENST00000680280.1:n.1716G>C
ENST00000680349.1:n.2862G>C
ENST00000680403.1:c.4198G>C	ENSP00000505677.1:p.Glu1400Gln
ENST00000680564.1:c.3964G>C	ENSP00000505582.1:p.Glu1322Gln
ENST00000680590.1:c.*2593G>C	ENSP00000505350.1:n.*2593G>C
ENST00000680597.1:c.946G>C
ENST00000680739.1:c.1228G>C
ENST00000680773.1:n.2714G>C
ENST00000680806.1:c.*3516G>C	ENSP00000506418.1:n.*3516G>C
ENST00000680997.1:n.2145G>C
ENST00000681608.1:n.2058G>C
ENST00000681625.1:c.*1545G>C	ENSP00000505555.1:n.*1545G>C
ENST00000681648.1:n.2264G>C
ENST00000270301.11:c.4198G>C	ENSP00000270301.6:p.Glu1400Gln
ENST00000401500.6:c.4213G>C	ENSP00000384792.1:p.Glu1405Gln
ENST00000587391.5:c.*4073G>C	ENSP00000465525.1:n.*4073G>C
NM_001083961.1:c.4213G>C	NP_001077430.1:p.Glu1405Gln
NM_173636.4:c.4198G>C	NP_775907.4:p.Glu1400Gln
XM_005258809.2:c.4102G>C	XP_005258866.1:p.Glu1368Gln
XM_011526837.1:c.4198G>C	XP_011525139.1:p.Glu1400Gln
XM_011526838.1:c.3964G>C	XP_011525140.1:p.Glu1322Gln
XM_011526839.1:c.3862G>C	XP_011525141.1:p.Glu1288Gln
XM_011526840.1:c.3205G>C	XP_011525142.1:p.Glu1069Gln
XM_011526841.1:c.2791G>C	XP_011525143.1:p.Glu931Gln
XM_011526842.1:c.2644G>C	XP_011525144.1:p.Glu882Gln
XM_011526843.1:c.1960G>C	XP_011525145.1:p.Glu654Gln
XM_011526844.1:c.1960G>C	XP_011525146.1:p.Glu654Gln
XM_011526840.2:c.3205G>C	XP_011525142.1:p.Glu1069Gln
XM_011526841.2:c.2791G>C	XP_011525143.1:p.Glu931Gln
XM_011526844.2:c.1960G>C	XP_011525146.1:p.Glu654Gln
XM_017026665.1:c.4213G>C	XP_016882154.1:p.Glu1405Gln
NM_001083961.2:c.4213G>C MANE Select	NP_001077430.1:p.Glu1405Gln
NM_173636.5:c.4198G>C	NP_775907.4:p.Glu1400Gln