Canonical Allele Identifier: CA405460414

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595450C>G (hg19) ; chr19:g.36104548C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104548C>G , CM000681.2:g.36104548C>G	GRCh38
NC_000019.9:g.36595450C>G , CM000681.1:g.36595450C>G	GRCh37
NC_000019.8:g.41287290C>G	NCBI36
NG_028101.1:g.54668C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4169C>G	ENSP00000270301.6:p.Ala1390Gly
ENST00000401500.7:c.4184C>G MANE Select	ENSP00000384792.1:p.Ala1395Gly
ENST00000587391.6:c.*4044C>G	ENSP00000465525.1:n.*4044C>G
ENST00000679357.1:c.2264C>G
ENST00000679598.1:c.929C>G
ENST00000679682.1:c.4169C>G	ENSP00000506226.1:p.Ala1390Gly
ENST00000679714.1:c.4178C>G	ENSP00000506627.1:p.Ala1393Gly
ENST00000679757.1:c.3833C>G	ENSP00000505158.1:p.Ala1278Gly
ENST00000679858.1:c.*3566C>G	ENSP00000505655.1:n.*3566C>G
ENST00000680211.1:c.785C>G	ENSP00000506102.1:p.Ala262Gly
ENST00000680280.1:n.1687C>G
ENST00000680349.1:n.2833C>G
ENST00000680403.1:c.4169C>G	ENSP00000505677.1:p.Ala1390Gly
ENST00000680564.1:c.3935C>G	ENSP00000505582.1:p.Ala1312Gly
ENST00000680590.1:c.*2564C>G	ENSP00000505350.1:n.*2564C>G
ENST00000680597.1:c.917C>G
ENST00000680739.1:c.1199C>G
ENST00000680773.1:n.2685C>G
ENST00000680806.1:c.*3487C>G	ENSP00000506418.1:n.*3487C>G
ENST00000680997.1:n.2116C>G
ENST00000681608.1:n.2029C>G
ENST00000681625.1:c.*1516C>G	ENSP00000505555.1:n.*1516C>G
ENST00000681648.1:n.2235C>G
ENST00000270301.11:c.4169C>G	ENSP00000270301.6:p.Ala1390Gly
ENST00000401500.6:c.4184C>G	ENSP00000384792.1:p.Ala1395Gly
ENST00000587391.5:c.*4044C>G	ENSP00000465525.1:n.*4044C>G
NM_001083961.1:c.4184C>G	NP_001077430.1:p.Ala1395Gly
NM_173636.4:c.4169C>G	NP_775907.4:p.Ala1390Gly
XM_005258809.2:c.4073C>G	XP_005258866.1:p.Ala1358Gly
XM_011526837.1:c.4169C>G	XP_011525139.1:p.Ala1390Gly
XM_011526838.1:c.3935C>G	XP_011525140.1:p.Ala1312Gly
XM_011526839.1:c.3833C>G	XP_011525141.1:p.Ala1278Gly
XM_011526840.1:c.3176C>G	XP_011525142.1:p.Ala1059Gly
XM_011526841.1:c.2762C>G	XP_011525143.1:p.Ala921Gly
XM_011526842.1:c.2615C>G	XP_011525144.1:p.Ala872Gly
XM_011526843.1:c.1931C>G	XP_011525145.1:p.Ala644Gly
XM_011526844.1:c.1931C>G	XP_011525146.1:p.Ala644Gly
XM_011526840.2:c.3176C>G	XP_011525142.1:p.Ala1059Gly
XM_011526841.2:c.2762C>G	XP_011525143.1:p.Ala921Gly
XM_011526844.2:c.1931C>G	XP_011525146.1:p.Ala644Gly
XM_017026665.1:c.4184C>G	XP_016882154.1:p.Ala1395Gly
NM_001083961.2:c.4184C>G MANE Select	NP_001077430.1:p.Ala1395Gly
NM_173636.5:c.4169C>G	NP_775907.4:p.Ala1390Gly