Canonical Allele Identifier: CA405460416

Gene: WDR62

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4169C>T	ENSP00000270301.6:p.Ala1390Val
ENST00000401500.7:c.4184C>T MANE Select	ENSP00000384792.1:p.Ala1395Val
ENST00000587391.6:c.*4044C>T	ENSP00000465525.1:n.*4044C>T
ENST00000679357.1:c.2264C>T
ENST00000679598.1:c.929C>T
ENST00000679682.1:c.4169C>T	ENSP00000506226.1:p.Ala1390Val
ENST00000679714.1:c.4178C>T	ENSP00000506627.1:p.Ala1393Val
ENST00000679757.1:c.3833C>T	ENSP00000505158.1:p.Ala1278Val
ENST00000679858.1:c.*3566C>T	ENSP00000505655.1:n.*3566C>T
ENST00000680211.1:c.785C>T	ENSP00000506102.1:p.Ala262Val
ENST00000680280.1:n.1687C>T
ENST00000680349.1:n.2833C>T
ENST00000680403.1:c.4169C>T	ENSP00000505677.1:p.Ala1390Val
ENST00000680564.1:c.3935C>T	ENSP00000505582.1:p.Ala1312Val
ENST00000680590.1:c.*2564C>T	ENSP00000505350.1:n.*2564C>T
ENST00000680597.1:c.917C>T
ENST00000680739.1:c.1199C>T
ENST00000680773.1:n.2685C>T
ENST00000680806.1:c.*3487C>T	ENSP00000506418.1:n.*3487C>T
ENST00000680997.1:n.2116C>T
ENST00000681608.1:n.2029C>T
ENST00000681625.1:c.*1516C>T	ENSP00000505555.1:n.*1516C>T
ENST00000681648.1:n.2235C>T
ENST00000270301.11:c.4169C>T	ENSP00000270301.6:p.Ala1390Val
ENST00000401500.6:c.4184C>T	ENSP00000384792.1:p.Ala1395Val
ENST00000587391.5:c.*4044C>T	ENSP00000465525.1:n.*4044C>T
NM_001083961.1:c.4184C>T	NP_001077430.1:p.Ala1395Val
NM_173636.4:c.4169C>T	NP_775907.4:p.Ala1390Val
XM_005258809.2:c.4073C>T	XP_005258866.1:p.Ala1358Val
XM_011526837.1:c.4169C>T	XP_011525139.1:p.Ala1390Val
XM_011526838.1:c.3935C>T	XP_011525140.1:p.Ala1312Val
XM_011526839.1:c.3833C>T	XP_011525141.1:p.Ala1278Val
XM_011526840.1:c.3176C>T	XP_011525142.1:p.Ala1059Val
XM_011526841.1:c.2762C>T	XP_011525143.1:p.Ala921Val
XM_011526842.1:c.2615C>T	XP_011525144.1:p.Ala872Val
XM_011526843.1:c.1931C>T	XP_011525145.1:p.Ala644Val
XM_011526844.1:c.1931C>T	XP_011525146.1:p.Ala644Val
XM_011526840.2:c.3176C>T	XP_011525142.1:p.Ala1059Val
XM_011526841.2:c.2762C>T	XP_011525143.1:p.Ala921Val
XM_011526844.2:c.1931C>T	XP_011525146.1:p.Ala644Val
XM_017026665.1:c.4184C>T	XP_016882154.1:p.Ala1395Val
NM_001083961.2:c.4184C>T MANE Select	NP_001077430.1:p.Ala1395Val
NM_173636.5:c.4169C>T	NP_775907.4:p.Ala1390Val