Canonical Allele Identifier: CA405449418

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101732-G-T
• MyVariant Identifiers: chr19:g.36592634G>T (hg19) ; chr19:g.36101732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101732G>T , CM000681.2:g.36101732G>T	GRCh38
NC_000019.9:g.36592634G>T , CM000681.1:g.36592634G>T	GRCh37
NC_000019.8:g.41284474G>T	NCBI36
NG_028101.1:g.51852G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3040G>T	ENSP00000270301.6:p.Asp1014Tyr
ENST00000401500.7:c.3040G>T MANE Select	ENSP00000384792.1:p.Asp1014Tyr
ENST00000587391.6:c.*2076G>T	ENSP00000465525.1:n.*2076G>T
ENST00000679357.1:c.830G>T
ENST00000679422.1:c.762-282G>T
ENST00000679682.1:c.3025G>T	ENSP00000506226.1:p.Asp1009Tyr
ENST00000679714.1:c.3034G>T	ENSP00000506627.1:p.Asp1012Tyr
ENST00000679757.1:c.2689G>T	ENSP00000505158.1:p.Asp897Tyr
ENST00000679858.1:c.*2183G>T	ENSP00000505655.1:n.*2183G>T
ENST00000680211.1:c.-360G>T	ENSP00000506102.1:n.-360G>T
ENST00000680349.1:n.1023G>T
ENST00000680403.1:c.3040G>T	ENSP00000505677.1:p.Asp1014Tyr
ENST00000680564.1:c.2971+415G>T	ENSP00000505582.1:n.2971+415G>T
ENST00000680590.1:c.*1435G>T	ENSP00000505350.1:n.*1435G>T
ENST00000680773.1:n.717G>T
ENST00000680806.1:c.*1801-282G>T	ENSP00000506418.1:n.*1801-282G>T
ENST00000680997.1:n.387G>T
ENST00000681088.1:c.702G>T
ENST00000681625.1:c.*372G>T	ENSP00000505555.1:n.*372G>T
ENST00000270301.11:c.3040G>T	ENSP00000270301.6:p.Asp1014Tyr
ENST00000401500.6:c.3040G>T	ENSP00000384792.1:p.Asp1014Tyr
ENST00000587391.5:c.*2076G>T	ENSP00000465525.1:n.*2076G>T
NM_001083961.1:c.3040G>T	NP_001077430.1:p.Asp1014Tyr
NM_173636.4:c.3040G>T	NP_775907.4:p.Asp1014Tyr
XM_005258809.2:c.2972-282G>T	XP_005258866.1:n.2972-282G>T
XM_011526837.1:c.3025G>T	XP_011525139.1:p.Asp1009Tyr
XM_011526838.1:c.2971+415G>T	XP_011525140.1:n.2971+415G>T
XM_011526839.1:c.2689G>T	XP_011525141.1:p.Asp897Tyr
XM_011526840.1:c.2032G>T	XP_011525142.1:p.Asp678Tyr
XM_011526841.1:c.1618G>T	XP_011525143.1:p.Asp540Tyr
XM_011526842.1:c.1471G>T	XP_011525144.1:p.Asp491Tyr
XM_011526843.1:c.787G>T	XP_011525145.1:p.Asp263Tyr
XM_011526844.1:c.787G>T	XP_011525146.1:p.Asp263Tyr
XM_011526840.2:c.2032G>T	XP_011525142.1:p.Asp678Tyr
XM_011526841.2:c.1618G>T	XP_011525143.1:p.Asp540Tyr
XM_011526844.2:c.787G>T	XP_011525146.1:p.Asp263Tyr
XM_017026665.1:c.3040G>T	XP_016882154.1:p.Asp1014Tyr
NM_001083961.2:c.3040G>T MANE Select	NP_001077430.1:p.Asp1014Tyr
NM_173636.5:c.3040G>T	NP_775907.4:p.Asp1014Tyr