Canonical Allele Identifier: CA405449615

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101759-C-A
• MyVariant Identifiers: chr19:g.36592661C>A (hg19) ; chr19:g.36101759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101759C>A , CM000681.2:g.36101759C>A	GRCh38
NC_000019.9:g.36592661C>A , CM000681.1:g.36592661C>A	GRCh37
NC_000019.8:g.41284501C>A	NCBI36
NG_028101.1:g.51879C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3067C>A	ENSP00000270301.6:p.Leu1023Met
ENST00000401500.7:c.3067C>A MANE Select	ENSP00000384792.1:p.Leu1023Met
ENST00000587391.6:c.*2103C>A	ENSP00000465525.1:n.*2103C>A
ENST00000679357.1:c.857C>A
ENST00000679422.1:c.762-255C>A
ENST00000679682.1:c.3052C>A	ENSP00000506226.1:p.Leu1018Met
ENST00000679714.1:c.3061C>A	ENSP00000506627.1:p.Leu1021Met
ENST00000679757.1:c.2716C>A	ENSP00000505158.1:p.Leu906Met
ENST00000679858.1:c.*2210C>A	ENSP00000505655.1:n.*2210C>A
ENST00000680211.1:c.-333C>A	ENSP00000506102.1:n.-333C>A
ENST00000680349.1:n.1050C>A
ENST00000680403.1:c.3067C>A	ENSP00000505677.1:p.Leu1023Met
ENST00000680564.1:c.2971+442C>A	ENSP00000505582.1:n.2971+442C>A
ENST00000680590.1:c.*1462C>A	ENSP00000505350.1:n.*1462C>A
ENST00000680773.1:n.744C>A
ENST00000680806.1:c.*1801-255C>A	ENSP00000506418.1:n.*1801-255C>A
ENST00000680997.1:n.414C>A
ENST00000681088.1:c.729C>A
ENST00000681608.1:n.15C>A
ENST00000681625.1:c.*399C>A	ENSP00000505555.1:n.*399C>A
ENST00000270301.11:c.3067C>A	ENSP00000270301.6:p.Leu1023Met
ENST00000401500.6:c.3067C>A	ENSP00000384792.1:p.Leu1023Met
ENST00000587391.5:c.*2103C>A	ENSP00000465525.1:n.*2103C>A
NM_001083961.1:c.3067C>A	NP_001077430.1:p.Leu1023Met
NM_173636.4:c.3067C>A	NP_775907.4:p.Leu1023Met
XM_005258809.2:c.2972-255C>A	XP_005258866.1:n.2972-255C>A
XM_011526837.1:c.3052C>A	XP_011525139.1:p.Leu1018Met
XM_011526838.1:c.2971+442C>A	XP_011525140.1:n.2971+442C>A
XM_011526839.1:c.2716C>A	XP_011525141.1:p.Leu906Met
XM_011526840.1:c.2059C>A	XP_011525142.1:p.Leu687Met
XM_011526841.1:c.1645C>A	XP_011525143.1:p.Leu549Met
XM_011526842.1:c.1498C>A	XP_011525144.1:p.Leu500Met
XM_011526843.1:c.814C>A	XP_011525145.1:p.Leu272Met
XM_011526844.1:c.814C>A	XP_011525146.1:p.Leu272Met
XM_011526840.2:c.2059C>A	XP_011525142.1:p.Leu687Met
XM_011526841.2:c.1645C>A	XP_011525143.1:p.Leu549Met
XM_011526844.2:c.814C>A	XP_011525146.1:p.Leu272Met
XM_017026665.1:c.3067C>A	XP_016882154.1:p.Leu1023Met
NM_001083961.2:c.3067C>A MANE Select	NP_001077430.1:p.Leu1023Met
NM_173636.5:c.3067C>A	NP_775907.4:p.Leu1023Met