Canonical Allele Identifier: CA405450192

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102062-G-T
• MyVariant Identifiers: chr19:g.36592964G>T (hg19) ; chr19:g.36102062G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102062G>T , CM000681.2:g.36102062G>T	GRCh38
NC_000019.9:g.36592964G>T , CM000681.1:g.36592964G>T	GRCh37
NC_000019.8:g.41284804G>T	NCBI36
NG_028101.1:g.52182G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3131G>T	ENSP00000270301.6:p.Ser1044Ile
ENST00000401500.7:c.3131G>T MANE Select	ENSP00000384792.1:p.Ser1044Ile
ENST00000587391.6:c.*2406G>T	ENSP00000465525.1:n.*2406G>T
ENST00000679357.1:c.921G>T
ENST00000679422.1:c.810G>T
ENST00000679682.1:c.3116G>T	ENSP00000506226.1:p.Ser1039Ile
ENST00000679714.1:c.3125G>T	ENSP00000506627.1:p.Ser1042Ile
ENST00000679757.1:c.2780G>T	ENSP00000505158.1:p.Ser927Ile
ENST00000679858.1:c.*2513G>T	ENSP00000505655.1:n.*2513G>T
ENST00000680211.1:c.-269G>T	ENSP00000506102.1:n.-269G>T
ENST00000680349.1:n.1114G>T
ENST00000680403.1:c.3131G>T	ENSP00000505677.1:p.Ser1044Ile
ENST00000680564.1:c.2972-675G>T	ENSP00000505582.1:n.2972-675G>T
ENST00000680590.1:c.*1526G>T	ENSP00000505350.1:n.*1526G>T
ENST00000680739.1:c.49G>T
ENST00000680773.1:n.1047G>T
ENST00000680806.1:c.*1849G>T	ENSP00000506418.1:n.*1849G>T
ENST00000680997.1:n.478G>T
ENST00000681088.1:c.793G>T
ENST00000681608.1:n.79G>T
ENST00000681625.1:c.*463G>T	ENSP00000505555.1:n.*463G>T
ENST00000270301.11:c.3131G>T	ENSP00000270301.6:p.Ser1044Ile
ENST00000401500.6:c.3131G>T	ENSP00000384792.1:p.Ser1044Ile
ENST00000587391.5:c.*2406G>T	ENSP00000465525.1:n.*2406G>T
NM_001083961.1:c.3131G>T	NP_001077430.1:p.Ser1044Ile
NM_173636.4:c.3131G>T	NP_775907.4:p.Ser1044Ile
XM_005258809.2:c.3020G>T	XP_005258866.1:p.Ser1007Ile
XM_011526837.1:c.3116G>T	XP_011525139.1:p.Ser1039Ile
XM_011526838.1:c.2972-675G>T	XP_011525140.1:n.2972-675G>T
XM_011526839.1:c.2780G>T	XP_011525141.1:p.Ser927Ile
XM_011526840.1:c.2123G>T	XP_011525142.1:p.Ser708Ile
XM_011526841.1:c.1709G>T	XP_011525143.1:p.Ser570Ile
XM_011526842.1:c.1562G>T	XP_011525144.1:p.Ser521Ile
XM_011526843.1:c.878G>T	XP_011525145.1:p.Ser293Ile
XM_011526844.1:c.878G>T	XP_011525146.1:p.Ser293Ile
XM_011526840.2:c.2123G>T	XP_011525142.1:p.Ser708Ile
XM_011526841.2:c.1709G>T	XP_011525143.1:p.Ser570Ile
XM_011526844.2:c.878G>T	XP_011525146.1:p.Ser293Ile
XM_017026665.1:c.3131G>T	XP_016882154.1:p.Ser1044Ile
NM_001083961.2:c.3131G>T MANE Select	NP_001077430.1:p.Ser1044Ile
NM_173636.5:c.3131G>T	NP_775907.4:p.Ser1044Ile