Canonical Allele Identifier: CA995509161

Gene: WDR62

Linked Data

• dbSNP Id: rs1973364084
• gnomAD v3: 19-36101834-CAATGTCT-C
• gnomAD v4: 19-36101834-CAATGTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101837_36101843del , CM000681.2:g.36101837_36101843del	GRCh38
NC_000019.9:g.36592739_36592745del , CM000681.1:g.36592739_36592745del	GRCh37
NC_000019.8:g.41284579_41284585del	NCBI36
NG_028101.1:g.51957_51963del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3082+63_3082+69del	ENSP00000270301.6:n.3082+63_3082+69del
ENST00000401500.7:c.3082+63_3082+69del MANE Select	ENSP00000384792.1:n.3082+63_3082+69del
ENST00000587391.6:c.*2181_*2187del	ENSP00000465525.1:n.*2181_*2187del
ENST00000679357.1:c.872+63_872+69del
ENST00000679422.1:c.762-177_762-171del
ENST00000679682.1:c.3067+63_3067+69del	ENSP00000506226.1:n.3067+63_3067+69del
ENST00000679714.1:c.3076+63_3076+69del	ENSP00000506627.1:n.3076+63_3076+69del
ENST00000679757.1:c.2731+63_2731+69del	ENSP00000505158.1:n.2731+63_2731+69del
ENST00000679858.1:c.*2288_*2294del	ENSP00000505655.1:n.*2288_*2294del
ENST00000680211.1:c.-318+63_-318+69del	ENSP00000506102.1:n.-318+63_-318+69del
ENST00000680349.1:n.1065+63_1065+69del
ENST00000680403.1:c.3082+63_3082+69del	ENSP00000505677.1:n.3082+63_3082+69del
ENST00000680564.1:c.2971+520_2971+526del	ENSP00000505582.1:n.2971+520_2971+526del
ENST00000680590.1:c.*1477+63_*1477+69del	ENSP00000505350.1:n.*1477+63_*1477+69del
ENST00000680773.1:n.822_828del
ENST00000680806.1:c.*1801-177_*1801-171del	ENSP00000506418.1:n.*1801-177_*1801-171del
ENST00000680997.1:n.429+63_429+69del
ENST00000681088.1:c.744+63_744+69del
ENST00000681608.1:n.30+63_30+69del
ENST00000681625.1:c.*414+63_*414+69del	ENSP00000505555.1:n.*414+63_*414+69del
ENST00000270301.11:c.3082+63_3082+69del	ENSP00000270301.6:n.3082+63_3082+69del
ENST00000401500.6:c.3082+63_3082+69del	ENSP00000384792.1:n.3082+63_3082+69del
ENST00000587391.5:c.*2181_*2187del	ENSP00000465525.1:n.*2181_*2187del
NM_001083961.1:c.3082+63_3082+69del	NP_001077430.1:n.3082+63_3082+69del
NM_173636.4:c.3082+63_3082+69del	NP_775907.4:n.3082+63_3082+69del
XM_005258809.2:c.2972-177_2972-171del	XP_005258866.1:n.2972-177_2972-171del
XM_011526837.1:c.3067+63_3067+69del	XP_011525139.1:n.3067+63_3067+69del
XM_011526838.1:c.2971+520_2971+526del	XP_011525140.1:n.2971+520_2971+526del
XM_011526839.1:c.2731+63_2731+69del	XP_011525141.1:n.2731+63_2731+69del
XM_011526840.1:c.2074+63_2074+69del	XP_011525142.1:n.2074+63_2074+69del
XM_011526841.1:c.1660+63_1660+69del	XP_011525143.1:n.1660+63_1660+69del
XM_011526842.1:c.1513+63_1513+69del	XP_011525144.1:n.1513+63_1513+69del
XM_011526843.1:c.829+63_829+69del	XP_011525145.1:n.829+63_829+69del
XM_011526844.1:c.829+63_829+69del	XP_011525146.1:n.829+63_829+69del
XM_011526840.2:c.2074+63_2074+69del	XP_011525142.1:n.2074+63_2074+69del
XM_011526841.2:c.1660+63_1660+69del	XP_011525143.1:n.1660+63_1660+69del
XM_011526844.2:c.829+63_829+69del	XP_011525146.1:n.829+63_829+69del
XM_017026665.1:c.3082+63_3082+69del	XP_016882154.1:n.3082+63_3082+69del
NM_001083961.2:c.3082+63_3082+69del MANE Select	NP_001077430.1:n.3082+63_3082+69del
NM_173636.5:c.3082+63_3082+69del	NP_775907.4:n.3082+63_3082+69del