Canonical Allele Identifier: CA405450254

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592973G>C (hg19) ; chr19:g.36102071G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102071G>C , CM000681.2:g.36102071G>C	GRCh38
NC_000019.9:g.36592973G>C , CM000681.1:g.36592973G>C	GRCh37
NC_000019.8:g.41284813G>C	NCBI36
NG_028101.1:g.52191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3140G>C	ENSP00000270301.6:p.Ser1047Thr
ENST00000401500.7:c.3140G>C MANE Select	ENSP00000384792.1:p.Ser1047Thr
ENST00000587391.6:c.*2415G>C	ENSP00000465525.1:n.*2415G>C
ENST00000679357.1:c.930G>C
ENST00000679422.1:c.819G>C
ENST00000679682.1:c.3125G>C	ENSP00000506226.1:p.Ser1042Thr
ENST00000679714.1:c.3134G>C	ENSP00000506627.1:p.Ser1045Thr
ENST00000679757.1:c.2789G>C	ENSP00000505158.1:p.Ser930Thr
ENST00000679858.1:c.*2522G>C	ENSP00000505655.1:n.*2522G>C
ENST00000680211.1:c.-260G>C	ENSP00000506102.1:n.-260G>C
ENST00000680349.1:n.1123G>C
ENST00000680403.1:c.3140G>C	ENSP00000505677.1:p.Ser1047Thr
ENST00000680564.1:c.2972-666G>C	ENSP00000505582.1:n.2972-666G>C
ENST00000680590.1:c.*1535G>C	ENSP00000505350.1:n.*1535G>C
ENST00000680739.1:c.58G>C
ENST00000680773.1:n.1056G>C
ENST00000680806.1:c.*1858G>C	ENSP00000506418.1:n.*1858G>C
ENST00000680997.1:n.487G>C
ENST00000681088.1:c.802G>C
ENST00000681608.1:n.88G>C
ENST00000681625.1:c.*472G>C	ENSP00000505555.1:n.*472G>C
ENST00000270301.11:c.3140G>C	ENSP00000270301.6:p.Ser1047Thr
ENST00000401500.6:c.3140G>C	ENSP00000384792.1:p.Ser1047Thr
ENST00000587391.5:c.*2415G>C	ENSP00000465525.1:n.*2415G>C
NM_001083961.1:c.3140G>C	NP_001077430.1:p.Ser1047Thr
NM_173636.4:c.3140G>C	NP_775907.4:p.Ser1047Thr
XM_005258809.2:c.3029G>C	XP_005258866.1:p.Ser1010Thr
XM_011526837.1:c.3125G>C	XP_011525139.1:p.Ser1042Thr
XM_011526838.1:c.2972-666G>C	XP_011525140.1:n.2972-666G>C
XM_011526839.1:c.2789G>C	XP_011525141.1:p.Ser930Thr
XM_011526840.1:c.2132G>C	XP_011525142.1:p.Ser711Thr
XM_011526841.1:c.1718G>C	XP_011525143.1:p.Ser573Thr
XM_011526842.1:c.1571G>C	XP_011525144.1:p.Ser524Thr
XM_011526843.1:c.887G>C	XP_011525145.1:p.Ser296Thr
XM_011526844.1:c.887G>C	XP_011525146.1:p.Ser296Thr
XM_011526840.2:c.2132G>C	XP_011525142.1:p.Ser711Thr
XM_011526841.2:c.1718G>C	XP_011525143.1:p.Ser573Thr
XM_011526844.2:c.887G>C	XP_011525146.1:p.Ser296Thr
XM_017026665.1:c.3140G>C	XP_016882154.1:p.Ser1047Thr
NM_001083961.2:c.3140G>C MANE Select	NP_001077430.1:p.Ser1047Thr
NM_173636.5:c.3140G>C	NP_775907.4:p.Ser1047Thr