Canonical Allele Identifier: CA507107585

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593025T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102123T>C , CM000681.2:g.36102123T>C	GRCh38
NC_000019.9:g.36593025T>C , CM000681.1:g.36593025T>C	GRCh37
NC_000019.8:g.41284865T>C	NCBI36
NG_028101.1:g.52243T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3192T>C	ENSP00000270301.6:p.Phe1064=
ENST00000401500.7:c.3192T>C MANE Select	ENSP00000384792.1:p.Phe1064=
ENST00000587391.6:c.*2467T>C	ENSP00000465525.1:n.*2467T>C
ENST00000679357.1:c.982T>C
ENST00000679422.1:c.871T>C
ENST00000679682.1:c.3177T>C	ENSP00000506226.1:p.Phe1059=
ENST00000679714.1:c.3186T>C	ENSP00000506627.1:p.Phe1062=
ENST00000679757.1:c.2841T>C	ENSP00000505158.1:p.Phe947=
ENST00000679858.1:c.*2574T>C	ENSP00000505655.1:n.*2574T>C
ENST00000680211.1:c.-208T>C	ENSP00000506102.1:n.-208T>C
ENST00000680349.1:n.1175T>C
ENST00000680403.1:c.3192T>C	ENSP00000505677.1:p.Phe1064=
ENST00000680564.1:c.2972-614T>C	ENSP00000505582.1:n.2972-614T>C
ENST00000680590.1:c.*1587T>C	ENSP00000505350.1:n.*1587T>C
ENST00000680739.1:c.110T>C
ENST00000680773.1:n.1108T>C
ENST00000680806.1:c.*1910T>C	ENSP00000506418.1:n.*1910T>C
ENST00000680997.1:n.539T>C
ENST00000681088.1:c.854T>C
ENST00000681608.1:n.140T>C
ENST00000681625.1:c.*524T>C	ENSP00000505555.1:n.*524T>C
ENST00000270301.11:c.3192T>C	ENSP00000270301.6:p.Phe1064=
ENST00000401500.6:c.3192T>C	ENSP00000384792.1:p.Phe1064=
ENST00000587391.5:c.*2467T>C	ENSP00000465525.1:n.*2467T>C
NM_001083961.1:c.3192T>C	NP_001077430.1:p.Phe1064=
NM_173636.4:c.3192T>C	NP_775907.4:p.Phe1064=
XM_005258809.2:c.3081T>C	XP_005258866.1:p.Phe1027=
XM_011526837.1:c.3177T>C	XP_011525139.1:p.Phe1059=
XM_011526838.1:c.2972-614T>C	XP_011525140.1:n.2972-614T>C
XM_011526839.1:c.2841T>C	XP_011525141.1:p.Phe947=
XM_011526840.1:c.2184T>C	XP_011525142.1:p.Phe728=
XM_011526841.1:c.1770T>C	XP_011525143.1:p.Phe590=
XM_011526842.1:c.1623T>C	XP_011525144.1:p.Phe541=
XM_011526843.1:c.939T>C	XP_011525145.1:p.Phe313=
XM_011526844.1:c.939T>C	XP_011525146.1:p.Phe313=
XM_011526840.2:c.2184T>C	XP_011525142.1:p.Phe728=
XM_011526841.2:c.1770T>C	XP_011525143.1:p.Phe590=
XM_011526844.2:c.939T>C	XP_011525146.1:p.Phe313=
XM_017026665.1:c.3192T>C	XP_016882154.1:p.Phe1064=
NM_001083961.2:c.3192T>C MANE Select	NP_001077430.1:p.Phe1064=
NM_173636.5:c.3192T>C	NP_775907.4:p.Phe1064=