Canonical Allele Identifier: CA405451931

Gene: WDR62

Linked Data

• dbSNP Id: rs1170829156
• gnomAD v3: 19-36102802-C-T
• gnomAD v4: 19-36102802-C-T
• MyVariant Identifiers: chr19:g.36593704C>T (hg19) ; chr19:g.36102802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102802C>T , CM000681.2:g.36102802C>T	GRCh38
NC_000019.9:g.36593704C>T , CM000681.1:g.36593704C>T	GRCh37
NC_000019.8:g.41285544C>T	NCBI36
NG_028101.1:g.52922C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3271C>T	ENSP00000270301.6:p.Arg1091Cys
ENST00000401500.7:c.3286C>T MANE Select	ENSP00000384792.1:p.Arg1096Cys
ENST00000587391.6:c.*3146C>T	ENSP00000465525.1:n.*3146C>T
ENST00000679357.1:c.1366C>T
ENST00000679598.1:c.51C>T
ENST00000679682.1:c.3271C>T	ENSP00000506226.1:p.Arg1091Cys
ENST00000679714.1:c.3280C>T	ENSP00000506627.1:p.Arg1094Cys
ENST00000679757.1:c.2935C>T	ENSP00000505158.1:p.Arg979Cys
ENST00000679858.1:c.*2668C>T	ENSP00000505655.1:n.*2668C>T
ENST00000680211.1:c.-114C>T	ENSP00000506102.1:n.-114C>T
ENST00000680280.1:n.573C>T
ENST00000680349.1:n.1854C>T
ENST00000680403.1:c.3271C>T	ENSP00000505677.1:p.Arg1091Cys
ENST00000680564.1:c.3037C>T	ENSP00000505582.1:p.Arg1013Cys
ENST00000680590.1:c.*1666C>T	ENSP00000505350.1:n.*1666C>T
ENST00000680597.1:c.51C>T
ENST00000680739.1:c.301C>T
ENST00000680773.1:n.1787C>T
ENST00000680806.1:c.*2589C>T	ENSP00000506418.1:n.*2589C>T
ENST00000680997.1:n.1218C>T
ENST00000681608.1:n.819C>T
ENST00000681625.1:c.*618C>T	ENSP00000505555.1:n.*618C>T
ENST00000681648.1:n.585C>T
ENST00000270301.11:c.3271C>T	ENSP00000270301.6:p.Arg1091Cys
ENST00000401500.6:c.3286C>T	ENSP00000384792.1:p.Arg1096Cys
ENST00000587391.5:c.*3146C>T	ENSP00000465525.1:n.*3146C>T
NM_001083961.1:c.3286C>T	NP_001077430.1:p.Arg1096Cys
NM_173636.4:c.3271C>T	NP_775907.4:p.Arg1091Cys
XM_005258809.2:c.3175C>T	XP_005258866.1:p.Arg1059Cys
XM_011526837.1:c.3271C>T	XP_011525139.1:p.Arg1091Cys
XM_011526838.1:c.3037C>T	XP_011525140.1:p.Arg1013Cys
XM_011526839.1:c.2935C>T	XP_011525141.1:p.Arg979Cys
XM_011526840.1:c.2278C>T	XP_011525142.1:p.Arg760Cys
XM_011526841.1:c.1864C>T	XP_011525143.1:p.Arg622Cys
XM_011526842.1:c.1717C>T	XP_011525144.1:p.Arg573Cys
XM_011526843.1:c.1033C>T	XP_011525145.1:p.Arg345Cys
XM_011526844.1:c.1033C>T	XP_011525146.1:p.Arg345Cys
XM_011526840.2:c.2278C>T	XP_011525142.1:p.Arg760Cys
XM_011526841.2:c.1864C>T	XP_011525143.1:p.Arg622Cys
XM_011526844.2:c.1033C>T	XP_011525146.1:p.Arg345Cys
XM_017026665.1:c.3286C>T	XP_016882154.1:p.Arg1096Cys
NM_001083961.2:c.3286C>T MANE Select	NP_001077430.1:p.Arg1096Cys
NM_173636.5:c.3271C>T	NP_775907.4:p.Arg1091Cys