Canonical Allele Identifier: CA405450609

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593012T>G (hg19) ; chr19:g.36102110T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102110T>G , CM000681.2:g.36102110T>G	GRCh38
NC_000019.9:g.36593012T>G , CM000681.1:g.36593012T>G	GRCh37
NC_000019.8:g.41284852T>G	NCBI36
NG_028101.1:g.52230T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3179T>G	ENSP00000270301.6:p.Leu1060Arg
ENST00000401500.7:c.3179T>G MANE Select	ENSP00000384792.1:p.Leu1060Arg
ENST00000587391.6:c.*2454T>G	ENSP00000465525.1:n.*2454T>G
ENST00000679357.1:c.969T>G
ENST00000679422.1:c.858T>G
ENST00000679682.1:c.3164T>G	ENSP00000506226.1:p.Leu1055Arg
ENST00000679714.1:c.3173T>G	ENSP00000506627.1:p.Leu1058Arg
ENST00000679757.1:c.2828T>G	ENSP00000505158.1:p.Leu943Arg
ENST00000679858.1:c.*2561T>G	ENSP00000505655.1:n.*2561T>G
ENST00000680211.1:c.-221T>G	ENSP00000506102.1:n.-221T>G
ENST00000680349.1:n.1162T>G
ENST00000680403.1:c.3179T>G	ENSP00000505677.1:p.Leu1060Arg
ENST00000680564.1:c.2972-627T>G	ENSP00000505582.1:n.2972-627T>G
ENST00000680590.1:c.*1574T>G	ENSP00000505350.1:n.*1574T>G
ENST00000680739.1:c.97T>G
ENST00000680773.1:n.1095T>G
ENST00000680806.1:c.*1897T>G	ENSP00000506418.1:n.*1897T>G
ENST00000680997.1:n.526T>G
ENST00000681088.1:c.841T>G
ENST00000681608.1:n.127T>G
ENST00000681625.1:c.*511T>G	ENSP00000505555.1:n.*511T>G
ENST00000270301.11:c.3179T>G	ENSP00000270301.6:p.Leu1060Arg
ENST00000401500.6:c.3179T>G	ENSP00000384792.1:p.Leu1060Arg
ENST00000587391.5:c.*2454T>G	ENSP00000465525.1:n.*2454T>G
NM_001083961.1:c.3179T>G	NP_001077430.1:p.Leu1060Arg
NM_173636.4:c.3179T>G	NP_775907.4:p.Leu1060Arg
XM_005258809.2:c.3068T>G	XP_005258866.1:p.Leu1023Arg
XM_011526837.1:c.3164T>G	XP_011525139.1:p.Leu1055Arg
XM_011526838.1:c.2972-627T>G	XP_011525140.1:n.2972-627T>G
XM_011526839.1:c.2828T>G	XP_011525141.1:p.Leu943Arg
XM_011526840.1:c.2171T>G	XP_011525142.1:p.Leu724Arg
XM_011526841.1:c.1757T>G	XP_011525143.1:p.Leu586Arg
XM_011526842.1:c.1610T>G	XP_011525144.1:p.Leu537Arg
XM_011526843.1:c.926T>G	XP_011525145.1:p.Leu309Arg
XM_011526844.1:c.926T>G	XP_011525146.1:p.Leu309Arg
XM_011526840.2:c.2171T>G	XP_011525142.1:p.Leu724Arg
XM_011526841.2:c.1757T>G	XP_011525143.1:p.Leu586Arg
XM_011526844.2:c.926T>G	XP_011525146.1:p.Leu309Arg
XM_017026665.1:c.3179T>G	XP_016882154.1:p.Leu1060Arg
NM_001083961.2:c.3179T>G MANE Select	NP_001077430.1:p.Leu1060Arg
NM_173636.5:c.3179T>G	NP_775907.4:p.Leu1060Arg