Canonical Allele Identifier: CA405450430

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102089-C-G
• MyVariant Identifiers: chr19:g.36592991C>G (hg19) ; chr19:g.36102089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102089C>G , CM000681.2:g.36102089C>G	GRCh38
NC_000019.9:g.36592991C>G , CM000681.1:g.36592991C>G	GRCh37
NC_000019.8:g.41284831C>G	NCBI36
NG_028101.1:g.52209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3158C>G	ENSP00000270301.6:p.Thr1053Ser
ENST00000401500.7:c.3158C>G MANE Select	ENSP00000384792.1:p.Thr1053Ser
ENST00000587391.6:c.*2433C>G	ENSP00000465525.1:n.*2433C>G
ENST00000679357.1:c.948C>G
ENST00000679422.1:c.837C>G
ENST00000679682.1:c.3143C>G	ENSP00000506226.1:p.Thr1048Ser
ENST00000679714.1:c.3152C>G	ENSP00000506627.1:p.Thr1051Ser
ENST00000679757.1:c.2807C>G	ENSP00000505158.1:p.Thr936Ser
ENST00000679858.1:c.*2540C>G	ENSP00000505655.1:n.*2540C>G
ENST00000680211.1:c.-242C>G	ENSP00000506102.1:n.-242C>G
ENST00000680349.1:n.1141C>G
ENST00000680403.1:c.3158C>G	ENSP00000505677.1:p.Thr1053Ser
ENST00000680564.1:c.2972-648C>G	ENSP00000505582.1:n.2972-648C>G
ENST00000680590.1:c.*1553C>G	ENSP00000505350.1:n.*1553C>G
ENST00000680739.1:c.76C>G
ENST00000680773.1:n.1074C>G
ENST00000680806.1:c.*1876C>G	ENSP00000506418.1:n.*1876C>G
ENST00000680997.1:n.505C>G
ENST00000681088.1:c.820C>G
ENST00000681608.1:n.106C>G
ENST00000681625.1:c.*490C>G	ENSP00000505555.1:n.*490C>G
ENST00000270301.11:c.3158C>G	ENSP00000270301.6:p.Thr1053Ser
ENST00000401500.6:c.3158C>G	ENSP00000384792.1:p.Thr1053Ser
ENST00000587391.5:c.*2433C>G	ENSP00000465525.1:n.*2433C>G
NM_001083961.1:c.3158C>G	NP_001077430.1:p.Thr1053Ser
NM_173636.4:c.3158C>G	NP_775907.4:p.Thr1053Ser
XM_005258809.2:c.3047C>G	XP_005258866.1:p.Thr1016Ser
XM_011526837.1:c.3143C>G	XP_011525139.1:p.Thr1048Ser
XM_011526838.1:c.2972-648C>G	XP_011525140.1:n.2972-648C>G
XM_011526839.1:c.2807C>G	XP_011525141.1:p.Thr936Ser
XM_011526840.1:c.2150C>G	XP_011525142.1:p.Thr717Ser
XM_011526841.1:c.1736C>G	XP_011525143.1:p.Thr579Ser
XM_011526842.1:c.1589C>G	XP_011525144.1:p.Thr530Ser
XM_011526843.1:c.905C>G	XP_011525145.1:p.Thr302Ser
XM_011526844.1:c.905C>G	XP_011525146.1:p.Thr302Ser
XM_011526840.2:c.2150C>G	XP_011525142.1:p.Thr717Ser
XM_011526841.2:c.1736C>G	XP_011525143.1:p.Thr579Ser
XM_011526844.2:c.905C>G	XP_011525146.1:p.Thr302Ser
XM_017026665.1:c.3158C>G	XP_016882154.1:p.Thr1053Ser
NM_001083961.2:c.3158C>G MANE Select	NP_001077430.1:p.Thr1053Ser
NM_173636.5:c.3158C>G	NP_775907.4:p.Thr1053Ser