Canonical Allele Identifier: CA2584644437

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102042-GTCCCTGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102043_36102050del , CM000681.2:g.36102043_36102050del	GRCh38
NC_000019.9:g.36592945_36592952del , CM000681.1:g.36592945_36592952del	GRCh37
NC_000019.8:g.41284785_41284792del	NCBI36
NG_028101.1:g.52163_52170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3112_3119del	ENSP00000270301.6:p.Ser1038ArgfsTer25
ENST00000401500.7:c.3112_3119del MANE Select	ENSP00000384792.1:p.Ser1038ArgfsTer25
ENST00000587391.6:c.*2387_*2394del	ENSP00000465525.1:n.*2387_*2394del
ENST00000679357.1:c.902_909del
ENST00000679422.1:c.791_798del
ENST00000679682.1:c.3097_3104del	ENSP00000506226.1:p.Ser1033ArgfsTer25
ENST00000679714.1:c.3106_3113del	ENSP00000506627.1:p.Ser1036ArgfsTer25
ENST00000679757.1:c.2761_2768del	ENSP00000505158.1:p.Ser921ArgfsTer25
ENST00000679858.1:c.*2494_*2501del	ENSP00000505655.1:n.*2494_*2501del
ENST00000680211.1:c.-288_-281del	ENSP00000506102.1:n.-288_-281del
ENST00000680349.1:n.1095_1102del
ENST00000680403.1:c.3112_3119del	ENSP00000505677.1:p.Ser1038ArgfsTer25
ENST00000680564.1:c.2972-694_2972-687del	ENSP00000505582.1:n.2972-694_2972-687del
ENST00000680590.1:c.*1507_*1514del	ENSP00000505350.1:n.*1507_*1514del
ENST00000680739.1:c.30_37del
ENST00000680773.1:n.1028_1035del
ENST00000680806.1:c.*1830_*1837del	ENSP00000506418.1:n.*1830_*1837del
ENST00000680997.1:n.459_466del
ENST00000681088.1:c.774_781del
ENST00000681608.1:n.60_67del
ENST00000681625.1:c.*444_*451del	ENSP00000505555.1:n.*444_*451del
ENST00000270301.11:c.3112_3119del	ENSP00000270301.6:p.Ser1038ArgfsTer25
ENST00000401500.6:c.3112_3119del	ENSP00000384792.1:p.Ser1038ArgfsTer25
ENST00000587391.5:c.*2387_*2394del	ENSP00000465525.1:n.*2387_*2394del
NM_001083961.1:c.3112_3119del	NP_001077430.1:p.Ser1038ArgfsTer25
NM_173636.4:c.3112_3119del	NP_775907.4:p.Ser1038ArgfsTer25
XM_005258809.2:c.3001_3008del	XP_005258866.1:p.Ser1001ArgfsTer25
XM_011526837.1:c.3097_3104del	XP_011525139.1:p.Ser1033ArgfsTer25
XM_011526838.1:c.2972-694_2972-687del	XP_011525140.1:n.2972-694_2972-687del
XM_011526839.1:c.2761_2768del	XP_011525141.1:p.Ser921ArgfsTer25
XM_011526840.1:c.2104_2111del	XP_011525142.1:p.Ser702ArgfsTer25
XM_011526841.1:c.1690_1697del	XP_011525143.1:p.Ser564ArgfsTer25
XM_011526842.1:c.1543_1550del	XP_011525144.1:p.Ser515ArgfsTer25
XM_011526843.1:c.859_866del	XP_011525145.1:p.Ser287ArgfsTer25
XM_011526844.1:c.859_866del	XP_011525146.1:p.Ser287ArgfsTer25
XM_011526840.2:c.2104_2111del	XP_011525142.1:p.Ser702ArgfsTer25
XM_011526841.2:c.1690_1697del	XP_011525143.1:p.Ser564ArgfsTer25
XM_011526844.2:c.859_866del	XP_011525146.1:p.Ser287ArgfsTer25
XM_017026665.1:c.3112_3119del	XP_016882154.1:p.Ser1038ArgfsTer25
NM_001083961.2:c.3112_3119del MANE Select	NP_001077430.1:p.Ser1038ArgfsTer25
NM_173636.5:c.3112_3119del	NP_775907.4:p.Ser1038ArgfsTer25