Canonical Allele Identifier: CA507107534

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592971C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102069C>A , CM000681.2:g.36102069C>A	GRCh38
NC_000019.9:g.36592971C>A , CM000681.1:g.36592971C>A	GRCh37
NC_000019.8:g.41284811C>A	NCBI36
NG_028101.1:g.52189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3138C>A	ENSP00000270301.6:p.Pro1046=
ENST00000401500.7:c.3138C>A MANE Select	ENSP00000384792.1:p.Pro1046=
ENST00000587391.6:c.*2413C>A	ENSP00000465525.1:n.*2413C>A
ENST00000679357.1:c.928C>A
ENST00000679422.1:c.817C>A
ENST00000679682.1:c.3123C>A	ENSP00000506226.1:p.Pro1041=
ENST00000679714.1:c.3132C>A	ENSP00000506627.1:p.Pro1044=
ENST00000679757.1:c.2787C>A	ENSP00000505158.1:p.Pro929=
ENST00000679858.1:c.*2520C>A	ENSP00000505655.1:n.*2520C>A
ENST00000680211.1:c.-262C>A	ENSP00000506102.1:n.-262C>A
ENST00000680349.1:n.1121C>A
ENST00000680403.1:c.3138C>A	ENSP00000505677.1:p.Pro1046=
ENST00000680564.1:c.2972-668C>A	ENSP00000505582.1:n.2972-668C>A
ENST00000680590.1:c.*1533C>A	ENSP00000505350.1:n.*1533C>A
ENST00000680739.1:c.56C>A
ENST00000680773.1:n.1054C>A
ENST00000680806.1:c.*1856C>A	ENSP00000506418.1:n.*1856C>A
ENST00000680997.1:n.485C>A
ENST00000681088.1:c.800C>A
ENST00000681608.1:n.86C>A
ENST00000681625.1:c.*470C>A	ENSP00000505555.1:n.*470C>A
ENST00000270301.11:c.3138C>A	ENSP00000270301.6:p.Pro1046=
ENST00000401500.6:c.3138C>A	ENSP00000384792.1:p.Pro1046=
ENST00000587391.5:c.*2413C>A	ENSP00000465525.1:n.*2413C>A
NM_001083961.1:c.3138C>A	NP_001077430.1:p.Pro1046=
NM_173636.4:c.3138C>A	NP_775907.4:p.Pro1046=
XM_005258809.2:c.3027C>A	XP_005258866.1:p.Pro1009=
XM_011526837.1:c.3123C>A	XP_011525139.1:p.Pro1041=
XM_011526838.1:c.2972-668C>A	XP_011525140.1:n.2972-668C>A
XM_011526839.1:c.2787C>A	XP_011525141.1:p.Pro929=
XM_011526840.1:c.2130C>A	XP_011525142.1:p.Pro710=
XM_011526841.1:c.1716C>A	XP_011525143.1:p.Pro572=
XM_011526842.1:c.1569C>A	XP_011525144.1:p.Pro523=
XM_011526843.1:c.885C>A	XP_011525145.1:p.Pro295=
XM_011526844.1:c.885C>A	XP_011525146.1:p.Pro295=
XM_011526840.2:c.2130C>A	XP_011525142.1:p.Pro710=
XM_011526841.2:c.1716C>A	XP_011525143.1:p.Pro572=
XM_011526844.2:c.885C>A	XP_011525146.1:p.Pro295=
XM_017026665.1:c.3138C>A	XP_016882154.1:p.Pro1046=
NM_001083961.2:c.3138C>A MANE Select	NP_001077430.1:p.Pro1046=
NM_173636.5:c.3138C>A	NP_775907.4:p.Pro1046=