Canonical Allele Identifier: CA507107577

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102108-C-T
• COSMIC: COSM4405457
• MyVariant Identifiers: chr19:g.36593010C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102108C>T , CM000681.2:g.36102108C>T	GRCh38
NC_000019.9:g.36593010C>T , CM000681.1:g.36593010C>T	GRCh37
NC_000019.8:g.41284850C>T	NCBI36
NG_028101.1:g.52228C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3177C>T	ENSP00000270301.6:p.Phe1059=
ENST00000401500.7:c.3177C>T MANE Select	ENSP00000384792.1:p.Phe1059=
ENST00000587391.6:c.*2452C>T	ENSP00000465525.1:n.*2452C>T
ENST00000679357.1:c.967C>T
ENST00000679422.1:c.856C>T
ENST00000679682.1:c.3162C>T	ENSP00000506226.1:p.Phe1054=
ENST00000679714.1:c.3171C>T	ENSP00000506627.1:p.Phe1057=
ENST00000679757.1:c.2826C>T	ENSP00000505158.1:p.Phe942=
ENST00000679858.1:c.*2559C>T	ENSP00000505655.1:n.*2559C>T
ENST00000680211.1:c.-223C>T	ENSP00000506102.1:n.-223C>T
ENST00000680349.1:n.1160C>T
ENST00000680403.1:c.3177C>T	ENSP00000505677.1:p.Phe1059=
ENST00000680564.1:c.2972-629C>T	ENSP00000505582.1:n.2972-629C>T
ENST00000680590.1:c.*1572C>T	ENSP00000505350.1:n.*1572C>T
ENST00000680739.1:c.95C>T
ENST00000680773.1:n.1093C>T
ENST00000680806.1:c.*1895C>T	ENSP00000506418.1:n.*1895C>T
ENST00000680997.1:n.524C>T
ENST00000681088.1:c.839C>T
ENST00000681608.1:n.125C>T
ENST00000681625.1:c.*509C>T	ENSP00000505555.1:n.*509C>T
ENST00000270301.11:c.3177C>T	ENSP00000270301.6:p.Phe1059=
ENST00000401500.6:c.3177C>T	ENSP00000384792.1:p.Phe1059=
ENST00000587391.5:c.*2452C>T	ENSP00000465525.1:n.*2452C>T
NM_001083961.1:c.3177C>T	NP_001077430.1:p.Phe1059=
NM_173636.4:c.3177C>T	NP_775907.4:p.Phe1059=
XM_005258809.2:c.3066C>T	XP_005258866.1:p.Phe1022=
XM_011526837.1:c.3162C>T	XP_011525139.1:p.Phe1054=
XM_011526838.1:c.2972-629C>T	XP_011525140.1:n.2972-629C>T
XM_011526839.1:c.2826C>T	XP_011525141.1:p.Phe942=
XM_011526840.1:c.2169C>T	XP_011525142.1:p.Phe723=
XM_011526841.1:c.1755C>T	XP_011525143.1:p.Phe585=
XM_011526842.1:c.1608C>T	XP_011525144.1:p.Phe536=
XM_011526843.1:c.924C>T	XP_011525145.1:p.Phe308=
XM_011526844.1:c.924C>T	XP_011525146.1:p.Phe308=
XM_011526840.2:c.2169C>T	XP_011525142.1:p.Phe723=
XM_011526841.2:c.1755C>T	XP_011525143.1:p.Phe585=
XM_011526844.2:c.924C>T	XP_011525146.1:p.Phe308=
XM_017026665.1:c.3177C>T	XP_016882154.1:p.Phe1059=
NM_001083961.2:c.3177C>T MANE Select	NP_001077430.1:p.Phe1059=
NM_173636.5:c.3177C>T	NP_775907.4:p.Phe1059=