Canonical Allele Identifier: CA405450798

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593032C>G (hg19) ; chr19:g.36102130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102130C>G , CM000681.2:g.36102130C>G	GRCh38
NC_000019.9:g.36593032C>G , CM000681.1:g.36593032C>G	GRCh37
NC_000019.8:g.41284872C>G	NCBI36
NG_028101.1:g.52250C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3199C>G	ENSP00000270301.6:p.Leu1067Val
ENST00000401500.7:c.3199C>G MANE Select	ENSP00000384792.1:p.Leu1067Val
ENST00000587391.6:c.*2474C>G	ENSP00000465525.1:n.*2474C>G
ENST00000679357.1:c.989C>G
ENST00000679422.1:c.878C>G
ENST00000679682.1:c.3184C>G	ENSP00000506226.1:p.Leu1062Val
ENST00000679714.1:c.3193C>G	ENSP00000506627.1:p.Leu1065Val
ENST00000679757.1:c.2848C>G	ENSP00000505158.1:p.Leu950Val
ENST00000679858.1:c.*2581C>G	ENSP00000505655.1:n.*2581C>G
ENST00000680211.1:c.-201C>G	ENSP00000506102.1:n.-201C>G
ENST00000680349.1:n.1182C>G
ENST00000680403.1:c.3199C>G	ENSP00000505677.1:p.Leu1067Val
ENST00000680564.1:c.2972-607C>G	ENSP00000505582.1:n.2972-607C>G
ENST00000680590.1:c.*1594C>G	ENSP00000505350.1:n.*1594C>G
ENST00000680739.1:c.117C>G
ENST00000680773.1:n.1115C>G
ENST00000680806.1:c.*1917C>G	ENSP00000506418.1:n.*1917C>G
ENST00000680997.1:n.546C>G
ENST00000681088.1:c.861C>G
ENST00000681608.1:n.147C>G
ENST00000681625.1:c.*531C>G	ENSP00000505555.1:n.*531C>G
ENST00000270301.11:c.3199C>G	ENSP00000270301.6:p.Leu1067Val
ENST00000401500.6:c.3199C>G	ENSP00000384792.1:p.Leu1067Val
ENST00000587391.5:c.*2474C>G	ENSP00000465525.1:n.*2474C>G
NM_001083961.1:c.3199C>G	NP_001077430.1:p.Leu1067Val
NM_173636.4:c.3199C>G	NP_775907.4:p.Leu1067Val
XM_005258809.2:c.3088C>G	XP_005258866.1:p.Leu1030Val
XM_011526837.1:c.3184C>G	XP_011525139.1:p.Leu1062Val
XM_011526838.1:c.2972-607C>G	XP_011525140.1:n.2972-607C>G
XM_011526839.1:c.2848C>G	XP_011525141.1:p.Leu950Val
XM_011526840.1:c.2191C>G	XP_011525142.1:p.Leu731Val
XM_011526841.1:c.1777C>G	XP_011525143.1:p.Leu593Val
XM_011526842.1:c.1630C>G	XP_011525144.1:p.Leu544Val
XM_011526843.1:c.946C>G	XP_011525145.1:p.Leu316Val
XM_011526844.1:c.946C>G	XP_011525146.1:p.Leu316Val
XM_011526840.2:c.2191C>G	XP_011525142.1:p.Leu731Val
XM_011526841.2:c.1777C>G	XP_011525143.1:p.Leu593Val
XM_011526844.2:c.946C>G	XP_011525146.1:p.Leu316Val
XM_017026665.1:c.3199C>G	XP_016882154.1:p.Leu1067Val
NM_001083961.2:c.3199C>G MANE Select	NP_001077430.1:p.Leu1067Val
NM_173636.5:c.3199C>G	NP_775907.4:p.Leu1067Val