Canonical Allele Identifier: CA405449965

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102029-C-T
• MyVariant Identifiers: chr19:g.36592931C>T (hg19) ; chr19:g.36102029C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102029C>T , CM000681.2:g.36102029C>T	GRCh38
NC_000019.9:g.36592931C>T , CM000681.1:g.36592931C>T	GRCh37
NC_000019.8:g.41284771C>T	NCBI36
NG_028101.1:g.52149C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3098C>T	ENSP00000270301.6:p.Thr1033Ile
ENST00000401500.7:c.3098C>T MANE Select	ENSP00000384792.1:p.Thr1033Ile
ENST00000587391.6:c.*2373C>T	ENSP00000465525.1:n.*2373C>T
ENST00000679357.1:c.888C>T
ENST00000679422.1:c.777C>T
ENST00000679682.1:c.3083C>T	ENSP00000506226.1:p.Thr1028Ile
ENST00000679714.1:c.3092C>T	ENSP00000506627.1:p.Thr1031Ile
ENST00000679757.1:c.2747C>T	ENSP00000505158.1:p.Thr916Ile
ENST00000679858.1:c.*2480C>T	ENSP00000505655.1:n.*2480C>T
ENST00000680211.1:c.-302C>T	ENSP00000506102.1:n.-302C>T
ENST00000680349.1:n.1081C>T
ENST00000680403.1:c.3098C>T	ENSP00000505677.1:p.Thr1033Ile
ENST00000680564.1:c.2972-708C>T	ENSP00000505582.1:n.2972-708C>T
ENST00000680590.1:c.*1493C>T	ENSP00000505350.1:n.*1493C>T
ENST00000680739.1:c.16C>T
ENST00000680773.1:n.1014C>T
ENST00000680806.1:c.*1816C>T	ENSP00000506418.1:n.*1816C>T
ENST00000680997.1:n.445C>T
ENST00000681088.1:c.760C>T
ENST00000681608.1:n.46C>T
ENST00000681625.1:c.*430C>T	ENSP00000505555.1:n.*430C>T
ENST00000270301.11:c.3098C>T	ENSP00000270301.6:p.Thr1033Ile
ENST00000401500.6:c.3098C>T	ENSP00000384792.1:p.Thr1033Ile
ENST00000587391.5:c.*2373C>T	ENSP00000465525.1:n.*2373C>T
NM_001083961.1:c.3098C>T	NP_001077430.1:p.Thr1033Ile
NM_173636.4:c.3098C>T	NP_775907.4:p.Thr1033Ile
XM_005258809.2:c.2987C>T	XP_005258866.1:p.Thr996Ile
XM_011526837.1:c.3083C>T	XP_011525139.1:p.Thr1028Ile
XM_011526838.1:c.2972-708C>T	XP_011525140.1:n.2972-708C>T
XM_011526839.1:c.2747C>T	XP_011525141.1:p.Thr916Ile
XM_011526840.1:c.2090C>T	XP_011525142.1:p.Thr697Ile
XM_011526841.1:c.1676C>T	XP_011525143.1:p.Thr559Ile
XM_011526842.1:c.1529C>T	XP_011525144.1:p.Thr510Ile
XM_011526843.1:c.845C>T	XP_011525145.1:p.Thr282Ile
XM_011526844.1:c.845C>T	XP_011525146.1:p.Thr282Ile
XM_011526840.2:c.2090C>T	XP_011525142.1:p.Thr697Ile
XM_011526841.2:c.1676C>T	XP_011525143.1:p.Thr559Ile
XM_011526844.2:c.845C>T	XP_011525146.1:p.Thr282Ile
XM_017026665.1:c.3098C>T	XP_016882154.1:p.Thr1033Ile
NM_001083961.2:c.3098C>T MANE Select	NP_001077430.1:p.Thr1033Ile
NM_173636.5:c.3098C>T	NP_775907.4:p.Thr1033Ile