Canonical Allele Identifier: CA405460750

Gene: WDR62

Linked Data

• dbSNP Id: rs768909004
• gnomAD v3: 19-36104587-C-A
• gnomAD v4: 19-36104587-C-A
• MyVariant Identifiers: chr19:g.36595489C>A (hg19) ; chr19:g.36104587C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104587C>A , CM000681.2:g.36104587C>A	GRCh38
NC_000019.9:g.36595489C>A , CM000681.1:g.36595489C>A	GRCh37
NC_000019.8:g.41287329C>A	NCBI36
NG_028101.1:g.54707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4208C>A	ENSP00000270301.6:p.Pro1403His
ENST00000401500.7:c.4223C>A MANE Select	ENSP00000384792.1:p.Pro1408His
ENST00000587391.6:c.*4083C>A	ENSP00000465525.1:n.*4083C>A
ENST00000679357.1:c.2303C>A
ENST00000679598.1:c.968C>A
ENST00000679682.1:c.4208C>A	ENSP00000506226.1:p.Pro1403His
ENST00000679714.1:c.4217C>A	ENSP00000506627.1:p.Pro1406His
ENST00000679757.1:c.3872C>A	ENSP00000505158.1:p.Pro1291His
ENST00000679858.1:c.*3605C>A	ENSP00000505655.1:n.*3605C>A
ENST00000680211.1:c.824C>A	ENSP00000506102.1:p.Pro275His
ENST00000680280.1:n.1726C>A
ENST00000680349.1:n.2872C>A
ENST00000680403.1:c.4208C>A	ENSP00000505677.1:p.Pro1403His
ENST00000680564.1:c.3974C>A	ENSP00000505582.1:p.Pro1325His
ENST00000680590.1:c.*2603C>A	ENSP00000505350.1:n.*2603C>A
ENST00000680597.1:c.956C>A
ENST00000680739.1:c.1238C>A
ENST00000680773.1:n.2724C>A
ENST00000680806.1:c.*3526C>A	ENSP00000506418.1:n.*3526C>A
ENST00000680997.1:n.2155C>A
ENST00000681608.1:n.2068C>A
ENST00000681625.1:c.*1555C>A	ENSP00000505555.1:n.*1555C>A
ENST00000681648.1:n.2274C>A
ENST00000270301.11:c.4208C>A	ENSP00000270301.6:p.Pro1403His
ENST00000401500.6:c.4223C>A	ENSP00000384792.1:p.Pro1408His
ENST00000587391.5:c.*4083C>A	ENSP00000465525.1:n.*4083C>A
NM_001083961.1:c.4223C>A	NP_001077430.1:p.Pro1408His
NM_173636.4:c.4208C>A	NP_775907.4:p.Pro1403His
XM_005258809.2:c.4112C>A	XP_005258866.1:p.Pro1371His
XM_011526837.1:c.4208C>A	XP_011525139.1:p.Pro1403His
XM_011526838.1:c.3974C>A	XP_011525140.1:p.Pro1325His
XM_011526839.1:c.3872C>A	XP_011525141.1:p.Pro1291His
XM_011526840.1:c.3215C>A	XP_011525142.1:p.Pro1072His
XM_011526841.1:c.2801C>A	XP_011525143.1:p.Pro934His
XM_011526842.1:c.2654C>A	XP_011525144.1:p.Pro885His
XM_011526843.1:c.1970C>A	XP_011525145.1:p.Pro657His
XM_011526844.1:c.1970C>A	XP_011525146.1:p.Pro657His
XM_011526840.2:c.3215C>A	XP_011525142.1:p.Pro1072His
XM_011526841.2:c.2801C>A	XP_011525143.1:p.Pro934His
XM_011526844.2:c.1970C>A	XP_011525146.1:p.Pro657His
XM_017026665.1:c.4223C>A	XP_016882154.1:p.Pro1408His
NM_001083961.2:c.4223C>A MANE Select	NP_001077430.1:p.Pro1408His
NM_173636.5:c.4208C>A	NP_775907.4:p.Pro1403His