Canonical Allele Identifier: CA405450124

Gene: WDR62

Linked Data

• dbSNP Id: rs762605299
• gnomAD v2: 19-36592954-G-T
• gnomAD v4: 19-36102052-G-T
• MyVariant Identifiers: chr19:g.36592954G>T (hg19) ; chr19:g.36102052G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102052G>T , CM000681.2:g.36102052G>T	GRCh38
NC_000019.9:g.36592954G>T , CM000681.1:g.36592954G>T	GRCh37
NC_000019.8:g.41284794G>T	NCBI36
NG_028101.1:g.52172G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3121G>T	ENSP00000270301.6:p.Glu1041Ter
ENST00000401500.7:c.3121G>T MANE Select	ENSP00000384792.1:p.Glu1041Ter
ENST00000587391.6:c.*2396G>T	ENSP00000465525.1:n.*2396G>T
ENST00000679357.1:c.911G>T
ENST00000679422.1:c.800G>T
ENST00000679682.1:c.3106G>T	ENSP00000506226.1:p.Glu1036Ter
ENST00000679714.1:c.3115G>T	ENSP00000506627.1:p.Glu1039Ter
ENST00000679757.1:c.2770G>T	ENSP00000505158.1:p.Glu924Ter
ENST00000679858.1:c.*2503G>T	ENSP00000505655.1:n.*2503G>T
ENST00000680211.1:c.-279G>T	ENSP00000506102.1:n.-279G>T
ENST00000680349.1:n.1104G>T
ENST00000680403.1:c.3121G>T	ENSP00000505677.1:p.Glu1041Ter
ENST00000680564.1:c.2972-685G>T	ENSP00000505582.1:n.2972-685G>T
ENST00000680590.1:c.*1516G>T	ENSP00000505350.1:n.*1516G>T
ENST00000680739.1:c.39G>T
ENST00000680773.1:n.1037G>T
ENST00000680806.1:c.*1839G>T	ENSP00000506418.1:n.*1839G>T
ENST00000680997.1:n.468G>T
ENST00000681088.1:c.783G>T
ENST00000681608.1:n.69G>T
ENST00000681625.1:c.*453G>T	ENSP00000505555.1:n.*453G>T
ENST00000270301.11:c.3121G>T	ENSP00000270301.6:p.Glu1041Ter
ENST00000401500.6:c.3121G>T	ENSP00000384792.1:p.Glu1041Ter
ENST00000587391.5:c.*2396G>T	ENSP00000465525.1:n.*2396G>T
NM_001083961.1:c.3121G>T	NP_001077430.1:p.Glu1041Ter
NM_173636.4:c.3121G>T	NP_775907.4:p.Glu1041Ter
XM_005258809.2:c.3010G>T	XP_005258866.1:p.Glu1004Ter
XM_011526837.1:c.3106G>T	XP_011525139.1:p.Glu1036Ter
XM_011526838.1:c.2972-685G>T	XP_011525140.1:n.2972-685G>T
XM_011526839.1:c.2770G>T	XP_011525141.1:p.Glu924Ter
XM_011526840.1:c.2113G>T	XP_011525142.1:p.Glu705Ter
XM_011526841.1:c.1699G>T	XP_011525143.1:p.Glu567Ter
XM_011526842.1:c.1552G>T	XP_011525144.1:p.Glu518Ter
XM_011526843.1:c.868G>T	XP_011525145.1:p.Glu290Ter
XM_011526844.1:c.868G>T	XP_011525146.1:p.Glu290Ter
XM_011526840.2:c.2113G>T	XP_011525142.1:p.Glu705Ter
XM_011526841.2:c.1699G>T	XP_011525143.1:p.Glu567Ter
XM_011526844.2:c.868G>T	XP_011525146.1:p.Glu290Ter
XM_017026665.1:c.3121G>T	XP_016882154.1:p.Glu1041Ter
NM_001083961.2:c.3121G>T MANE Select	NP_001077430.1:p.Glu1041Ter
NM_173636.5:c.3121G>T	NP_775907.4:p.Glu1041Ter