Canonical Allele Identifier: CA2814265345

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102151_36102152insAGCTCTTCCCC , CM000681.2:g.36102151_36102152insAGCTCTTCCCC	GRCh38
NC_000019.9:g.36593053_36593054insAGCTCTTCCCC , CM000681.1:g.36593053_36593054insAGCTCTTCCCC	GRCh37
NC_000019.8:g.41284893_41284894insAGCTCTTCCCC	NCBI36
NG_028101.1:g.52271_52272insAGCTCTTCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3220_3220+1insAGCTCTTCCCC	ENSP00000270301.6:n.3220_3220+1insAGCTCTTCCCC
ENST00000401500.7:c.3220_3220+1insAGCTCTTCCCC MANE Select	ENSP00000384792.1:n.3220_3220+1insAGCTCTTCCCC
ENST00000587391.6:c.*2495_*2496insAGCTCTTCCCC	ENSP00000465525.1:n.*2495_*2496insAGCTCTTCCCC
ENST00000679357.1:c.1010_1010+1insAGCTCTTCCCC
ENST00000679682.1:c.3205_3205+1insAGCTCTTCCCC	ENSP00000506226.1:n.3205_3205+1insAGCTCTTCCCC
ENST00000679714.1:c.3214_3214+1insAGCTCTTCCCC	ENSP00000506627.1:n.3214_3214+1insAGCTCTTCCCC
ENST00000679757.1:c.2869_2869+1insAGCTCTTCCCC	ENSP00000505158.1:n.2869_2869+1insAGCTCTTCCCC
ENST00000679858.1:c.*2602_*2602+1insAGCTCTTCCCC	ENSP00000505655.1:n.*2602_*2602+1insAGCTCTTCCCC
ENST00000680211.1:c.-180_-180+1insAGCTCTTCCCC	ENSP00000506102.1:n.-180_-180+1insAGCTCTTCCCC
ENST00000680349.1:n.1203_1204insAGCTCTTCCCC
ENST00000680403.1:c.3220_3220+1insAGCTCTTCCCC	ENSP00000505677.1:n.3220_3220+1insAGCTCTTCCCC
ENST00000680564.1:c.2972-586_2972-585insAGCTCTTCCCC	ENSP00000505582.1:n.2972-586_2972-585insAGCTCTTCCCC
ENST00000680590.1:c.*1615_*1615+1insAGCTCTTCCCC	ENSP00000505350.1:n.*1615_*1615+1insAGCTCTTCCCC
ENST00000680739.1:c.138_139insAGCTCTTCCCC
ENST00000680773.1:n.1136_1137insAGCTCTTCCCC
ENST00000680806.1:c.*1938_*1939insAGCTCTTCCCC	ENSP00000506418.1:n.*1938_*1939insAGCTCTTCCCC
ENST00000680997.1:n.567_568insAGCTCTTCCCC
ENST00000681608.1:n.168_169insAGCTCTTCCCC
ENST00000681625.1:c.*552_*552+1insAGCTCTTCCCC	ENSP00000505555.1:n.*552_*552+1insAGCTCTTCCCC
ENST00000270301.11:c.3220_3220+1insAGCTCTTCCCC	ENSP00000270301.6:n.3220_3220+1insAGCTCTTCCCC
ENST00000401500.6:c.3220_3220+1insAGCTCTTCCCC	ENSP00000384792.1:n.3220_3220+1insAGCTCTTCCCC
ENST00000587391.5:c.*2495_*2496insAGCTCTTCCCC	ENSP00000465525.1:n.*2495_*2496insAGCTCTTCCCC
NM_001083961.1:c.3220_3220+1insAGCTCTTCCCC	NP_001077430.1:n.3220_3220+1insAGCTCTTCCCC
NM_173636.4:c.3220_3220+1insAGCTCTTCCCC	NP_775907.4:n.3220_3220+1insAGCTCTTCCCC
XM_005258809.2:c.3109_3109+1insAGCTCTTCCCC	XP_005258866.1:n.3109_3109+1insAGCTCTTCCCC
XM_011526837.1:c.3205_3205+1insAGCTCTTCCCC	XP_011525139.1:n.3205_3205+1insAGCTCTTCCCC
XM_011526838.1:c.2972-586_2972-585insAGCTCTTCCCC	XP_011525140.1:n.2972-586_2972-585insAGCTCTTCCCC
XM_011526839.1:c.2869_2869+1insAGCTCTTCCCC	XP_011525141.1:n.2869_2869+1insAGCTCTTCCCC
XM_011526840.1:c.2212_2212+1insAGCTCTTCCCC	XP_011525142.1:n.2212_2212+1insAGCTCTTCCCC
XM_011526841.1:c.1798_1798+1insAGCTCTTCCCC	XP_011525143.1:n.1798_1798+1insAGCTCTTCCCC
XM_011526842.1:c.1651_1651+1insAGCTCTTCCCC	XP_011525144.1:n.1651_1651+1insAGCTCTTCCCC
XM_011526843.1:c.967_967+1insAGCTCTTCCCC	XP_011525145.1:n.967_967+1insAGCTCTTCCCC
XM_011526844.1:c.967_967+1insAGCTCTTCCCC	XP_011525146.1:n.967_967+1insAGCTCTTCCCC
XM_011526840.2:c.2212_2212+1insAGCTCTTCCCC	XP_011525142.1:n.2212_2212+1insAGCTCTTCCCC
XM_011526841.2:c.1798_1798+1insAGCTCTTCCCC	XP_011525143.1:n.1798_1798+1insAGCTCTTCCCC
XM_011526844.2:c.967_967+1insAGCTCTTCCCC	XP_011525146.1:n.967_967+1insAGCTCTTCCCC
XM_017026665.1:c.3220_3220+1insAGCTCTTCCCC	XP_016882154.1:n.3220_3220+1insAGCTCTTCCCC
NM_001083961.2:c.3220_3220+1insAGCTCTTCCCC MANE Select	NP_001077430.1:n.3220_3220+1insAGCTCTTCCCC
NM_173636.5:c.3220_3220+1insAGCTCTTCCCC	NP_775907.4:n.3220_3220+1insAGCTCTTCCCC