Canonical Allele Identifier: CA405450578

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102106-T-C
• MyVariant Identifiers: chr19:g.36593008T>C (hg19) ; chr19:g.36102106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102106T>C , CM000681.2:g.36102106T>C	GRCh38
NC_000019.9:g.36593008T>C , CM000681.1:g.36593008T>C	GRCh37
NC_000019.8:g.41284848T>C	NCBI36
NG_028101.1:g.52226T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3175T>C	ENSP00000270301.6:p.Phe1059Leu
ENST00000401500.7:c.3175T>C MANE Select	ENSP00000384792.1:p.Phe1059Leu
ENST00000587391.6:c.*2450T>C	ENSP00000465525.1:n.*2450T>C
ENST00000679357.1:c.965T>C
ENST00000679422.1:c.854T>C
ENST00000679682.1:c.3160T>C	ENSP00000506226.1:p.Phe1054Leu
ENST00000679714.1:c.3169T>C	ENSP00000506627.1:p.Phe1057Leu
ENST00000679757.1:c.2824T>C	ENSP00000505158.1:p.Phe942Leu
ENST00000679858.1:c.*2557T>C	ENSP00000505655.1:n.*2557T>C
ENST00000680211.1:c.-225T>C	ENSP00000506102.1:n.-225T>C
ENST00000680349.1:n.1158T>C
ENST00000680403.1:c.3175T>C	ENSP00000505677.1:p.Phe1059Leu
ENST00000680564.1:c.2972-631T>C	ENSP00000505582.1:n.2972-631T>C
ENST00000680590.1:c.*1570T>C	ENSP00000505350.1:n.*1570T>C
ENST00000680739.1:c.93T>C
ENST00000680773.1:n.1091T>C
ENST00000680806.1:c.*1893T>C	ENSP00000506418.1:n.*1893T>C
ENST00000680997.1:n.522T>C
ENST00000681088.1:c.837T>C
ENST00000681608.1:n.123T>C
ENST00000681625.1:c.*507T>C	ENSP00000505555.1:n.*507T>C
ENST00000270301.11:c.3175T>C	ENSP00000270301.6:p.Phe1059Leu
ENST00000401500.6:c.3175T>C	ENSP00000384792.1:p.Phe1059Leu
ENST00000587391.5:c.*2450T>C	ENSP00000465525.1:n.*2450T>C
NM_001083961.1:c.3175T>C	NP_001077430.1:p.Phe1059Leu
NM_173636.4:c.3175T>C	NP_775907.4:p.Phe1059Leu
XM_005258809.2:c.3064T>C	XP_005258866.1:p.Phe1022Leu
XM_011526837.1:c.3160T>C	XP_011525139.1:p.Phe1054Leu
XM_011526838.1:c.2972-631T>C	XP_011525140.1:n.2972-631T>C
XM_011526839.1:c.2824T>C	XP_011525141.1:p.Phe942Leu
XM_011526840.1:c.2167T>C	XP_011525142.1:p.Phe723Leu
XM_011526841.1:c.1753T>C	XP_011525143.1:p.Phe585Leu
XM_011526842.1:c.1606T>C	XP_011525144.1:p.Phe536Leu
XM_011526843.1:c.922T>C	XP_011525145.1:p.Phe308Leu
XM_011526844.1:c.922T>C	XP_011525146.1:p.Phe308Leu
XM_011526840.2:c.2167T>C	XP_011525142.1:p.Phe723Leu
XM_011526841.2:c.1753T>C	XP_011525143.1:p.Phe585Leu
XM_011526844.2:c.922T>C	XP_011525146.1:p.Phe308Leu
XM_017026665.1:c.3175T>C	XP_016882154.1:p.Phe1059Leu
NM_001083961.2:c.3175T>C MANE Select	NP_001077430.1:p.Phe1059Leu
NM_173636.5:c.3175T>C	NP_775907.4:p.Phe1059Leu