Canonical Allele Identifier: CA405452182

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102838C>T , CM000681.2:g.36102838C>T	GRCh38
NC_000019.9:g.36593740C>T , CM000681.1:g.36593740C>T	GRCh37
NC_000019.8:g.41285580C>T	NCBI36
NG_028101.1:g.52958C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3307C>T	ENSP00000270301.6:p.Gln1103Ter
ENST00000401500.7:c.3322C>T MANE Select	ENSP00000384792.1:p.Gln1108Ter
ENST00000587391.6:c.*3182C>T	ENSP00000465525.1:n.*3182C>T
ENST00000679357.1:c.1402C>T
ENST00000679598.1:c.87C>T
ENST00000679682.1:c.3307C>T	ENSP00000506226.1:p.Gln1103Ter
ENST00000679714.1:c.3316C>T	ENSP00000506627.1:p.Gln1106Ter
ENST00000679757.1:c.2971C>T	ENSP00000505158.1:p.Gln991Ter
ENST00000679858.1:c.*2704C>T	ENSP00000505655.1:n.*2704C>T
ENST00000680211.1:c.-78C>T	ENSP00000506102.1:n.-78C>T
ENST00000680280.1:n.609C>T
ENST00000680349.1:n.1890C>T
ENST00000680403.1:c.3307C>T	ENSP00000505677.1:p.Gln1103Ter
ENST00000680564.1:c.3073C>T	ENSP00000505582.1:p.Gln1025Ter
ENST00000680590.1:c.*1702C>T	ENSP00000505350.1:n.*1702C>T
ENST00000680597.1:c.87C>T
ENST00000680739.1:c.337C>T
ENST00000680773.1:n.1823C>T
ENST00000680806.1:c.*2625C>T	ENSP00000506418.1:n.*2625C>T
ENST00000680997.1:n.1254C>T
ENST00000681608.1:n.855C>T
ENST00000681625.1:c.*654C>T	ENSP00000505555.1:n.*654C>T
ENST00000681648.1:n.621C>T
ENST00000270301.11:c.3307C>T	ENSP00000270301.6:p.Gln1103Ter
ENST00000401500.6:c.3322C>T	ENSP00000384792.1:p.Gln1108Ter
ENST00000587391.5:c.*3182C>T	ENSP00000465525.1:n.*3182C>T
NM_001083961.1:c.3322C>T	NP_001077430.1:p.Gln1108Ter
NM_173636.4:c.3307C>T	NP_775907.4:p.Gln1103Ter
XM_005258809.2:c.3211C>T	XP_005258866.1:p.Gln1071Ter
XM_011526837.1:c.3307C>T	XP_011525139.1:p.Gln1103Ter
XM_011526838.1:c.3073C>T	XP_011525140.1:p.Gln1025Ter
XM_011526839.1:c.2971C>T	XP_011525141.1:p.Gln991Ter
XM_011526840.1:c.2314C>T	XP_011525142.1:p.Gln772Ter
XM_011526841.1:c.1900C>T	XP_011525143.1:p.Gln634Ter
XM_011526842.1:c.1753C>T	XP_011525144.1:p.Gln585Ter
XM_011526843.1:c.1069C>T	XP_011525145.1:p.Gln357Ter
XM_011526844.1:c.1069C>T	XP_011525146.1:p.Gln357Ter
XM_011526840.2:c.2314C>T	XP_011525142.1:p.Gln772Ter
XM_011526841.2:c.1900C>T	XP_011525143.1:p.Gln634Ter
XM_011526844.2:c.1069C>T	XP_011525146.1:p.Gln357Ter
XM_017026665.1:c.3322C>T	XP_016882154.1:p.Gln1108Ter
NM_001083961.2:c.3322C>T MANE Select	NP_001077430.1:p.Gln1108Ter
NM_173636.5:c.3307C>T	NP_775907.4:p.Gln1103Ter