Canonical Allele Identifier: CA2333970716

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101675T= , CM000681.2:g.36101675T=	GRCh38
NC_000019.9:g.36592577T= , CM000681.1:g.36592577T=	GRCh37
NC_000019.8:g.41284417T=	NCBI36
NG_028101.1:g.51795T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.2983T=	ENSP00000270301.6:p.Ser995=
ENST00000401500.7:c.2983T= MANE Select	ENSP00000384792.1:p.Ser995=
ENST00000587391.6:c.*2019T=	ENSP00000465525.1:n.*2019T=
ENST00000679357.1:c.773T=
ENST00000679422.1:c.762-339T=
ENST00000679682.1:c.2968T=	ENSP00000506226.1:p.Ser990=
ENST00000679714.1:c.2977T=	ENSP00000506627.1:p.Ser993=
ENST00000679757.1:c.2632T=	ENSP00000505158.1:p.Ser878=
ENST00000679858.1:c.*2126T=	ENSP00000505655.1:n.*2126T=
ENST00000680211.1:c.-417T=	ENSP00000506102.1:n.-417T=
ENST00000680349.1:n.966T=
ENST00000680403.1:c.2983T=	ENSP00000505677.1:p.Ser995=
ENST00000680564.1:c.2971+358T=	ENSP00000505582.1:n.2971+358T=
ENST00000680590.1:c.*1378T=	ENSP00000505350.1:n.*1378T=
ENST00000680773.1:n.660T=
ENST00000680806.1:c.*1801-339T=	ENSP00000506418.1:n.*1801-339T=
ENST00000680997.1:n.330T=
ENST00000681088.1:c.645T=
ENST00000681625.1:c.*315T=	ENSP00000505555.1:n.*315T=
ENST00000270301.11:c.2983T=	ENSP00000270301.6:p.Ser995=
ENST00000401500.6:c.2983T=	ENSP00000384792.1:p.Ser995=
ENST00000587391.5:c.*2019T=	ENSP00000465525.1:n.*2019T=
NM_001083961.1:c.2983T=	NP_001077430.1:p.Ser995=
NM_173636.4:c.2983T=	NP_775907.4:p.Ser995=
XM_005258809.2:c.2972-339T=	XP_005258866.1:n.2972-339T=
XM_011526837.1:c.2968T=	XP_011525139.1:p.Ser990=
XM_011526838.1:c.2971+358T=	XP_011525140.1:n.2971+358T=
XM_011526839.1:c.2632T=	XP_011525141.1:p.Ser878=
XM_011526840.1:c.1975T=	XP_011525142.1:p.Ser659=
XM_011526841.1:c.1561T=	XP_011525143.1:p.Ser521=
XM_011526842.1:c.1414T=	XP_011525144.1:p.Ser472=
XM_011526843.1:c.730T=	XP_011525145.1:p.Ser244=
XM_011526844.1:c.730T=	XP_011525146.1:p.Ser244=
XM_011526840.2:c.1975T=	XP_011525142.1:p.Ser659=
XM_011526841.2:c.1561T=	XP_011525143.1:p.Ser521=
XM_011526844.2:c.730T=	XP_011525146.1:p.Ser244=
XM_017026665.1:c.2983T=	XP_016882154.1:p.Ser995=
NM_001083961.2:c.2983T= MANE Select	NP_001077430.1:p.Ser995=
NM_173636.5:c.2983T=	NP_775907.4:p.Ser995=