Canonical Allele Identifier: CA405450518

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593001G>T (hg19) ; chr19:g.36102099G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102099G>T , CM000681.2:g.36102099G>T	GRCh38
NC_000019.9:g.36593001G>T , CM000681.1:g.36593001G>T	GRCh37
NC_000019.8:g.41284841G>T	NCBI36
NG_028101.1:g.52219G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3168G>T	ENSP00000270301.6:p.Gln1056His
ENST00000401500.7:c.3168G>T MANE Select	ENSP00000384792.1:p.Gln1056His
ENST00000587391.6:c.*2443G>T	ENSP00000465525.1:n.*2443G>T
ENST00000679357.1:c.958G>T
ENST00000679422.1:c.847G>T
ENST00000679682.1:c.3153G>T	ENSP00000506226.1:p.Gln1051His
ENST00000679714.1:c.3162G>T	ENSP00000506627.1:p.Gln1054His
ENST00000679757.1:c.2817G>T	ENSP00000505158.1:p.Gln939His
ENST00000679858.1:c.*2550G>T	ENSP00000505655.1:n.*2550G>T
ENST00000680211.1:c.-232G>T	ENSP00000506102.1:n.-232G>T
ENST00000680349.1:n.1151G>T
ENST00000680403.1:c.3168G>T	ENSP00000505677.1:p.Gln1056His
ENST00000680564.1:c.2972-638G>T	ENSP00000505582.1:n.2972-638G>T
ENST00000680590.1:c.*1563G>T	ENSP00000505350.1:n.*1563G>T
ENST00000680739.1:c.86G>T
ENST00000680773.1:n.1084G>T
ENST00000680806.1:c.*1886G>T	ENSP00000506418.1:n.*1886G>T
ENST00000680997.1:n.515G>T
ENST00000681088.1:c.830G>T
ENST00000681608.1:n.116G>T
ENST00000681625.1:c.*500G>T	ENSP00000505555.1:n.*500G>T
ENST00000270301.11:c.3168G>T	ENSP00000270301.6:p.Gln1056His
ENST00000401500.6:c.3168G>T	ENSP00000384792.1:p.Gln1056His
ENST00000587391.5:c.*2443G>T	ENSP00000465525.1:n.*2443G>T
NM_001083961.1:c.3168G>T	NP_001077430.1:p.Gln1056His
NM_173636.4:c.3168G>T	NP_775907.4:p.Gln1056His
XM_005258809.2:c.3057G>T	XP_005258866.1:p.Gln1019His
XM_011526837.1:c.3153G>T	XP_011525139.1:p.Gln1051His
XM_011526838.1:c.2972-638G>T	XP_011525140.1:n.2972-638G>T
XM_011526839.1:c.2817G>T	XP_011525141.1:p.Gln939His
XM_011526840.1:c.2160G>T	XP_011525142.1:p.Gln720His
XM_011526841.1:c.1746G>T	XP_011525143.1:p.Gln582His
XM_011526842.1:c.1599G>T	XP_011525144.1:p.Gln533His
XM_011526843.1:c.915G>T	XP_011525145.1:p.Gln305His
XM_011526844.1:c.915G>T	XP_011525146.1:p.Gln305His
XM_011526840.2:c.2160G>T	XP_011525142.1:p.Gln720His
XM_011526841.2:c.1746G>T	XP_011525143.1:p.Gln582His
XM_011526844.2:c.915G>T	XP_011525146.1:p.Gln305His
XM_017026665.1:c.3168G>T	XP_016882154.1:p.Gln1056His
NM_001083961.2:c.3168G>T MANE Select	NP_001077430.1:p.Gln1056His
NM_173636.5:c.3168G>T	NP_775907.4:p.Gln1056His