Canonical Allele Identifier: CA405460708

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104581-C-T
• MyVariant Identifiers: chr19:g.36595483C>T (hg19) ; chr19:g.36104581C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104581C>T , CM000681.2:g.36104581C>T	GRCh38
NC_000019.9:g.36595483C>T , CM000681.1:g.36595483C>T	GRCh37
NC_000019.8:g.41287323C>T	NCBI36
NG_028101.1:g.54701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4202C>T	ENSP00000270301.6:p.Ala1401Val
ENST00000401500.7:c.4217C>T MANE Select	ENSP00000384792.1:p.Ala1406Val
ENST00000587391.6:c.*4077C>T	ENSP00000465525.1:n.*4077C>T
ENST00000679357.1:c.2297C>T
ENST00000679598.1:c.962C>T
ENST00000679682.1:c.4202C>T	ENSP00000506226.1:p.Ala1401Val
ENST00000679714.1:c.4211C>T	ENSP00000506627.1:p.Ala1404Val
ENST00000679757.1:c.3866C>T	ENSP00000505158.1:p.Ala1289Val
ENST00000679858.1:c.*3599C>T	ENSP00000505655.1:n.*3599C>T
ENST00000680211.1:c.818C>T	ENSP00000506102.1:p.Ala273Val
ENST00000680280.1:n.1720C>T
ENST00000680349.1:n.2866C>T
ENST00000680403.1:c.4202C>T	ENSP00000505677.1:p.Ala1401Val
ENST00000680564.1:c.3968C>T	ENSP00000505582.1:p.Ala1323Val
ENST00000680590.1:c.*2597C>T	ENSP00000505350.1:n.*2597C>T
ENST00000680597.1:c.950C>T
ENST00000680739.1:c.1232C>T
ENST00000680773.1:n.2718C>T
ENST00000680806.1:c.*3520C>T	ENSP00000506418.1:n.*3520C>T
ENST00000680997.1:n.2149C>T
ENST00000681608.1:n.2062C>T
ENST00000681625.1:c.*1549C>T	ENSP00000505555.1:n.*1549C>T
ENST00000681648.1:n.2268C>T
ENST00000270301.11:c.4202C>T	ENSP00000270301.6:p.Ala1401Val
ENST00000401500.6:c.4217C>T	ENSP00000384792.1:p.Ala1406Val
ENST00000587391.5:c.*4077C>T	ENSP00000465525.1:n.*4077C>T
NM_001083961.1:c.4217C>T	NP_001077430.1:p.Ala1406Val
NM_173636.4:c.4202C>T	NP_775907.4:p.Ala1401Val
XM_005258809.2:c.4106C>T	XP_005258866.1:p.Ala1369Val
XM_011526837.1:c.4202C>T	XP_011525139.1:p.Ala1401Val
XM_011526838.1:c.3968C>T	XP_011525140.1:p.Ala1323Val
XM_011526839.1:c.3866C>T	XP_011525141.1:p.Ala1289Val
XM_011526840.1:c.3209C>T	XP_011525142.1:p.Ala1070Val
XM_011526841.1:c.2795C>T	XP_011525143.1:p.Ala932Val
XM_011526842.1:c.2648C>T	XP_011525144.1:p.Ala883Val
XM_011526843.1:c.1964C>T	XP_011525145.1:p.Ala655Val
XM_011526844.1:c.1964C>T	XP_011525146.1:p.Ala655Val
XM_011526840.2:c.3209C>T	XP_011525142.1:p.Ala1070Val
XM_011526841.2:c.2795C>T	XP_011525143.1:p.Ala932Val
XM_011526844.2:c.1964C>T	XP_011525146.1:p.Ala655Val
XM_017026665.1:c.4217C>T	XP_016882154.1:p.Ala1406Val
NM_001083961.2:c.4217C>T MANE Select	NP_001077430.1:p.Ala1406Val
NM_173636.5:c.4202C>T	NP_775907.4:p.Ala1401Val