Canonical Allele Identifier: CA405450185

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592963A>G (hg19) ; chr19:g.36102061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102061A>G , CM000681.2:g.36102061A>G	GRCh38
NC_000019.9:g.36592963A>G , CM000681.1:g.36592963A>G	GRCh37
NC_000019.8:g.41284803A>G	NCBI36
NG_028101.1:g.52181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3130A>G	ENSP00000270301.6:p.Ser1044Gly
ENST00000401500.7:c.3130A>G MANE Select	ENSP00000384792.1:p.Ser1044Gly
ENST00000587391.6:c.*2405A>G	ENSP00000465525.1:n.*2405A>G
ENST00000679357.1:c.920A>G
ENST00000679422.1:c.809A>G
ENST00000679682.1:c.3115A>G	ENSP00000506226.1:p.Ser1039Gly
ENST00000679714.1:c.3124A>G	ENSP00000506627.1:p.Ser1042Gly
ENST00000679757.1:c.2779A>G	ENSP00000505158.1:p.Ser927Gly
ENST00000679858.1:c.*2512A>G	ENSP00000505655.1:n.*2512A>G
ENST00000680211.1:c.-270A>G	ENSP00000506102.1:n.-270A>G
ENST00000680349.1:n.1113A>G
ENST00000680403.1:c.3130A>G	ENSP00000505677.1:p.Ser1044Gly
ENST00000680564.1:c.2972-676A>G	ENSP00000505582.1:n.2972-676A>G
ENST00000680590.1:c.*1525A>G	ENSP00000505350.1:n.*1525A>G
ENST00000680739.1:c.48A>G
ENST00000680773.1:n.1046A>G
ENST00000680806.1:c.*1848A>G	ENSP00000506418.1:n.*1848A>G
ENST00000680997.1:n.477A>G
ENST00000681088.1:c.792A>G
ENST00000681608.1:n.78A>G
ENST00000681625.1:c.*462A>G	ENSP00000505555.1:n.*462A>G
ENST00000270301.11:c.3130A>G	ENSP00000270301.6:p.Ser1044Gly
ENST00000401500.6:c.3130A>G	ENSP00000384792.1:p.Ser1044Gly
ENST00000587391.5:c.*2405A>G	ENSP00000465525.1:n.*2405A>G
NM_001083961.1:c.3130A>G	NP_001077430.1:p.Ser1044Gly
NM_173636.4:c.3130A>G	NP_775907.4:p.Ser1044Gly
XM_005258809.2:c.3019A>G	XP_005258866.1:p.Ser1007Gly
XM_011526837.1:c.3115A>G	XP_011525139.1:p.Ser1039Gly
XM_011526838.1:c.2972-676A>G	XP_011525140.1:n.2972-676A>G
XM_011526839.1:c.2779A>G	XP_011525141.1:p.Ser927Gly
XM_011526840.1:c.2122A>G	XP_011525142.1:p.Ser708Gly
XM_011526841.1:c.1708A>G	XP_011525143.1:p.Ser570Gly
XM_011526842.1:c.1561A>G	XP_011525144.1:p.Ser521Gly
XM_011526843.1:c.877A>G	XP_011525145.1:p.Ser293Gly
XM_011526844.1:c.877A>G	XP_011525146.1:p.Ser293Gly
XM_011526840.2:c.2122A>G	XP_011525142.1:p.Ser708Gly
XM_011526841.2:c.1708A>G	XP_011525143.1:p.Ser570Gly
XM_011526844.2:c.877A>G	XP_011525146.1:p.Ser293Gly
XM_017026665.1:c.3130A>G	XP_016882154.1:p.Ser1044Gly
NM_001083961.2:c.3130A>G MANE Select	NP_001077430.1:p.Ser1044Gly
NM_173636.5:c.3130A>G	NP_775907.4:p.Ser1044Gly