Canonical Allele Identifier: CA507318669

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595506C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104604C>T , CM000681.2:g.36104604C>T	GRCh38
NC_000019.9:g.36595506C>T , CM000681.1:g.36595506C>T	GRCh37
NC_000019.8:g.41287346C>T	NCBI36
NG_028101.1:g.54724C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4225C>T	ENSP00000270301.6:p.Leu1409=
ENST00000401500.7:c.4240C>T MANE Select	ENSP00000384792.1:p.Leu1414=
ENST00000587391.6:c.*4100C>T	ENSP00000465525.1:n.*4100C>T
ENST00000679357.1:c.2320C>T
ENST00000679598.1:c.985C>T
ENST00000679682.1:c.4225C>T	ENSP00000506226.1:p.Leu1409=
ENST00000679714.1:c.4234C>T	ENSP00000506627.1:p.Leu1412=
ENST00000679757.1:c.3889C>T	ENSP00000505158.1:p.Leu1297=
ENST00000679858.1:c.*3622C>T	ENSP00000505655.1:n.*3622C>T
ENST00000680211.1:c.841C>T	ENSP00000506102.1:p.Leu281=
ENST00000680280.1:n.1743C>T
ENST00000680349.1:n.2889C>T
ENST00000680403.1:c.4225C>T	ENSP00000505677.1:p.Leu1409=
ENST00000680564.1:c.3991C>T	ENSP00000505582.1:p.Leu1331=
ENST00000680590.1:c.*2620C>T	ENSP00000505350.1:n.*2620C>T
ENST00000680597.1:c.973C>T
ENST00000680739.1:c.1255C>T
ENST00000680773.1:n.2741C>T
ENST00000680806.1:c.*3543C>T	ENSP00000506418.1:n.*3543C>T
ENST00000680997.1:n.2172C>T
ENST00000681608.1:n.2085C>T
ENST00000681625.1:c.*1572C>T	ENSP00000505555.1:n.*1572C>T
ENST00000681648.1:n.2291C>T
ENST00000270301.11:c.4225C>T	ENSP00000270301.6:p.Leu1409=
ENST00000401500.6:c.4240C>T	ENSP00000384792.1:p.Leu1414=
ENST00000587391.5:c.*4100C>T	ENSP00000465525.1:n.*4100C>T
NM_001083961.1:c.4240C>T	NP_001077430.1:p.Leu1414=
NM_173636.4:c.4225C>T	NP_775907.4:p.Leu1409=
XM_005258809.2:c.4129C>T	XP_005258866.1:p.Leu1377=
XM_011526837.1:c.4225C>T	XP_011525139.1:p.Leu1409=
XM_011526838.1:c.3991C>T	XP_011525140.1:p.Leu1331=
XM_011526839.1:c.3889C>T	XP_011525141.1:p.Leu1297=
XM_011526840.1:c.3232C>T	XP_011525142.1:p.Leu1078=
XM_011526841.1:c.2818C>T	XP_011525143.1:p.Leu940=
XM_011526842.1:c.2671C>T	XP_011525144.1:p.Leu891=
XM_011526843.1:c.1987C>T	XP_011525145.1:p.Leu663=
XM_011526844.1:c.1987C>T	XP_011525146.1:p.Leu663=
XM_011526840.2:c.3232C>T	XP_011525142.1:p.Leu1078=
XM_011526841.2:c.2818C>T	XP_011525143.1:p.Leu940=
XM_011526844.2:c.1987C>T	XP_011525146.1:p.Leu663=
XM_017026665.1:c.4240C>T	XP_016882154.1:p.Leu1414=
NM_001083961.2:c.4240C>T MANE Select	NP_001077430.1:p.Leu1414=
NM_173636.5:c.4225C>T	NP_775907.4:p.Leu1409=