Canonical Allele Identifier: CA405450377

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102082-C-T
• MyVariant Identifiers: chr19:g.36592984C>T (hg19) ; chr19:g.36102082C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102082C>T , CM000681.2:g.36102082C>T	GRCh38
NC_000019.9:g.36592984C>T , CM000681.1:g.36592984C>T	GRCh37
NC_000019.8:g.41284824C>T	NCBI36
NG_028101.1:g.52202C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3151C>T	ENSP00000270301.6:p.Pro1051Ser
ENST00000401500.7:c.3151C>T MANE Select	ENSP00000384792.1:p.Pro1051Ser
ENST00000587391.6:c.*2426C>T	ENSP00000465525.1:n.*2426C>T
ENST00000679357.1:c.941C>T
ENST00000679422.1:c.830C>T
ENST00000679682.1:c.3136C>T	ENSP00000506226.1:p.Pro1046Ser
ENST00000679714.1:c.3145C>T	ENSP00000506627.1:p.Pro1049Ser
ENST00000679757.1:c.2800C>T	ENSP00000505158.1:p.Pro934Ser
ENST00000679858.1:c.*2533C>T	ENSP00000505655.1:n.*2533C>T
ENST00000680211.1:c.-249C>T	ENSP00000506102.1:n.-249C>T
ENST00000680349.1:n.1134C>T
ENST00000680403.1:c.3151C>T	ENSP00000505677.1:p.Pro1051Ser
ENST00000680564.1:c.2972-655C>T	ENSP00000505582.1:n.2972-655C>T
ENST00000680590.1:c.*1546C>T	ENSP00000505350.1:n.*1546C>T
ENST00000680739.1:c.69C>T
ENST00000680773.1:n.1067C>T
ENST00000680806.1:c.*1869C>T	ENSP00000506418.1:n.*1869C>T
ENST00000680997.1:n.498C>T
ENST00000681088.1:c.813C>T
ENST00000681608.1:n.99C>T
ENST00000681625.1:c.*483C>T	ENSP00000505555.1:n.*483C>T
ENST00000270301.11:c.3151C>T	ENSP00000270301.6:p.Pro1051Ser
ENST00000401500.6:c.3151C>T	ENSP00000384792.1:p.Pro1051Ser
ENST00000587391.5:c.*2426C>T	ENSP00000465525.1:n.*2426C>T
NM_001083961.1:c.3151C>T	NP_001077430.1:p.Pro1051Ser
NM_173636.4:c.3151C>T	NP_775907.4:p.Pro1051Ser
XM_005258809.2:c.3040C>T	XP_005258866.1:p.Pro1014Ser
XM_011526837.1:c.3136C>T	XP_011525139.1:p.Pro1046Ser
XM_011526838.1:c.2972-655C>T	XP_011525140.1:n.2972-655C>T
XM_011526839.1:c.2800C>T	XP_011525141.1:p.Pro934Ser
XM_011526840.1:c.2143C>T	XP_011525142.1:p.Pro715Ser
XM_011526841.1:c.1729C>T	XP_011525143.1:p.Pro577Ser
XM_011526842.1:c.1582C>T	XP_011525144.1:p.Pro528Ser
XM_011526843.1:c.898C>T	XP_011525145.1:p.Pro300Ser
XM_011526844.1:c.898C>T	XP_011525146.1:p.Pro300Ser
XM_011526840.2:c.2143C>T	XP_011525142.1:p.Pro715Ser
XM_011526841.2:c.1729C>T	XP_011525143.1:p.Pro577Ser
XM_011526844.2:c.898C>T	XP_011525146.1:p.Pro300Ser
XM_017026665.1:c.3151C>T	XP_016882154.1:p.Pro1051Ser
NM_001083961.2:c.3151C>T MANE Select	NP_001077430.1:p.Pro1051Ser
NM_173636.5:c.3151C>T	NP_775907.4:p.Pro1051Ser