Canonical Allele Identifier: CA507107494

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592926T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102024T>G , CM000681.2:g.36102024T>G	GRCh38
NC_000019.9:g.36592926T>G , CM000681.1:g.36592926T>G	GRCh37
NC_000019.8:g.41284766T>G	NCBI36
NG_028101.1:g.52144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3093T>G	ENSP00000270301.6:p.Gly1031=
ENST00000401500.7:c.3093T>G MANE Select	ENSP00000384792.1:p.Gly1031=
ENST00000587391.6:c.*2368T>G	ENSP00000465525.1:n.*2368T>G
ENST00000679357.1:c.883T>G
ENST00000679422.1:c.772T>G
ENST00000679682.1:c.3078T>G	ENSP00000506226.1:p.Gly1026=
ENST00000679714.1:c.3087T>G	ENSP00000506627.1:p.Gly1029=
ENST00000679757.1:c.2742T>G	ENSP00000505158.1:p.Gly914=
ENST00000679858.1:c.*2475T>G	ENSP00000505655.1:n.*2475T>G
ENST00000680211.1:c.-307T>G	ENSP00000506102.1:n.-307T>G
ENST00000680349.1:n.1076T>G
ENST00000680403.1:c.3093T>G	ENSP00000505677.1:p.Gly1031=
ENST00000680564.1:c.2971+707T>G	ENSP00000505582.1:n.2971+707T>G
ENST00000680590.1:c.*1488T>G	ENSP00000505350.1:n.*1488T>G
ENST00000680739.1:c.11T>G
ENST00000680773.1:n.1009T>G
ENST00000680806.1:c.*1811T>G	ENSP00000506418.1:n.*1811T>G
ENST00000680997.1:n.440T>G
ENST00000681088.1:c.755T>G
ENST00000681608.1:n.41T>G
ENST00000681625.1:c.*425T>G	ENSP00000505555.1:n.*425T>G
ENST00000270301.11:c.3093T>G	ENSP00000270301.6:p.Gly1031=
ENST00000401500.6:c.3093T>G	ENSP00000384792.1:p.Gly1031=
ENST00000587391.5:c.*2368T>G	ENSP00000465525.1:n.*2368T>G
NM_001083961.1:c.3093T>G	NP_001077430.1:p.Gly1031=
NM_173636.4:c.3093T>G	NP_775907.4:p.Gly1031=
XM_005258809.2:c.2982T>G	XP_005258866.1:p.Gly994=
XM_011526837.1:c.3078T>G	XP_011525139.1:p.Gly1026=
XM_011526838.1:c.2971+707T>G	XP_011525140.1:n.2971+707T>G
XM_011526839.1:c.2742T>G	XP_011525141.1:p.Gly914=
XM_011526840.1:c.2085T>G	XP_011525142.1:p.Gly695=
XM_011526841.1:c.1671T>G	XP_011525143.1:p.Gly557=
XM_011526842.1:c.1524T>G	XP_011525144.1:p.Gly508=
XM_011526843.1:c.840T>G	XP_011525145.1:p.Gly280=
XM_011526844.1:c.840T>G	XP_011525146.1:p.Gly280=
XM_011526840.2:c.2085T>G	XP_011525142.1:p.Gly695=
XM_011526841.2:c.1671T>G	XP_011525143.1:p.Gly557=
XM_011526844.2:c.840T>G	XP_011525146.1:p.Gly280=
XM_017026665.1:c.3093T>G	XP_016882154.1:p.Gly1031=
NM_001083961.2:c.3093T>G MANE Select	NP_001077430.1:p.Gly1031=
NM_173636.5:c.3093T>G	NP_775907.4:p.Gly1031=