Canonical Allele Identifier: CA405460368

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595439G>T (hg19) ; chr19:g.36104537G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104537G>T , CM000681.2:g.36104537G>T	GRCh38
NC_000019.9:g.36595439G>T , CM000681.1:g.36595439G>T	GRCh37
NC_000019.8:g.41287279G>T	NCBI36
NG_028101.1:g.54657G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4158G>T	ENSP00000270301.6:p.Gln1386His
ENST00000401500.7:c.4173G>T MANE Select	ENSP00000384792.1:p.Gln1391His
ENST00000587391.6:c.*4033G>T	ENSP00000465525.1:n.*4033G>T
ENST00000679357.1:c.2253G>T
ENST00000679598.1:c.919-1G>T
ENST00000679682.1:c.4158G>T	ENSP00000506226.1:p.Gln1386His
ENST00000679714.1:c.4167G>T	ENSP00000506627.1:p.Gln1389His
ENST00000679757.1:c.3822G>T	ENSP00000505158.1:p.Gln1274His
ENST00000679858.1:c.*3555G>T	ENSP00000505655.1:n.*3555G>T
ENST00000680211.1:c.774G>T	ENSP00000506102.1:p.Gln258His
ENST00000680280.1:n.1676G>T
ENST00000680349.1:n.2822G>T
ENST00000680403.1:c.4158G>T	ENSP00000505677.1:p.Gln1386His
ENST00000680564.1:c.3924G>T	ENSP00000505582.1:p.Gln1308His
ENST00000680590.1:c.*2553G>T	ENSP00000505350.1:n.*2553G>T
ENST00000680597.1:c.906G>T
ENST00000680739.1:c.1188G>T
ENST00000680773.1:n.2674G>T
ENST00000680806.1:c.*3476G>T	ENSP00000506418.1:n.*3476G>T
ENST00000680997.1:n.2105G>T
ENST00000681608.1:n.2018G>T
ENST00000681625.1:c.*1505G>T	ENSP00000505555.1:n.*1505G>T
ENST00000681648.1:n.2224G>T
ENST00000270301.11:c.4158G>T	ENSP00000270301.6:p.Gln1386His
ENST00000401500.6:c.4173G>T	ENSP00000384792.1:p.Gln1391His
ENST00000587391.5:c.*4033G>T	ENSP00000465525.1:n.*4033G>T
NM_001083961.1:c.4173G>T	NP_001077430.1:p.Gln1391His
NM_173636.4:c.4158G>T	NP_775907.4:p.Gln1386His
XM_005258809.2:c.4062G>T	XP_005258866.1:p.Gln1354His
XM_011526837.1:c.4158G>T	XP_011525139.1:p.Gln1386His
XM_011526838.1:c.3924G>T	XP_011525140.1:p.Gln1308His
XM_011526839.1:c.3822G>T	XP_011525141.1:p.Gln1274His
XM_011526840.1:c.3165G>T	XP_011525142.1:p.Gln1055His
XM_011526841.1:c.2751G>T	XP_011525143.1:p.Gln917His
XM_011526842.1:c.2604G>T	XP_011525144.1:p.Gln868His
XM_011526843.1:c.1920G>T	XP_011525145.1:p.Gln640His
XM_011526844.1:c.1920G>T	XP_011525146.1:p.Gln640His
XM_011526840.2:c.3165G>T	XP_011525142.1:p.Gln1055His
XM_011526841.2:c.2751G>T	XP_011525143.1:p.Gln917His
XM_011526844.2:c.1920G>T	XP_011525146.1:p.Gln640His
XM_017026665.1:c.4173G>T	XP_016882154.1:p.Gln1391His
NM_001083961.2:c.4173G>T MANE Select	NP_001077430.1:p.Gln1391His
NM_173636.5:c.4158G>T	NP_775907.4:p.Gln1386His