Canonical Allele Identifier: CA405450558

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593006A>C (hg19) ; chr19:g.36102104A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102104A>C , CM000681.2:g.36102104A>C	GRCh38
NC_000019.9:g.36593006A>C , CM000681.1:g.36593006A>C	GRCh37
NC_000019.8:g.41284846A>C	NCBI36
NG_028101.1:g.52224A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3173A>C	ENSP00000270301.6:p.Lys1058Thr
ENST00000401500.7:c.3173A>C MANE Select	ENSP00000384792.1:p.Lys1058Thr
ENST00000587391.6:c.*2448A>C	ENSP00000465525.1:n.*2448A>C
ENST00000679357.1:c.963A>C
ENST00000679422.1:c.852A>C
ENST00000679682.1:c.3158A>C	ENSP00000506226.1:p.Lys1053Thr
ENST00000679714.1:c.3167A>C	ENSP00000506627.1:p.Lys1056Thr
ENST00000679757.1:c.2822A>C	ENSP00000505158.1:p.Lys941Thr
ENST00000679858.1:c.*2555A>C	ENSP00000505655.1:n.*2555A>C
ENST00000680211.1:c.-227A>C	ENSP00000506102.1:n.-227A>C
ENST00000680349.1:n.1156A>C
ENST00000680403.1:c.3173A>C	ENSP00000505677.1:p.Lys1058Thr
ENST00000680564.1:c.2972-633A>C	ENSP00000505582.1:n.2972-633A>C
ENST00000680590.1:c.*1568A>C	ENSP00000505350.1:n.*1568A>C
ENST00000680739.1:c.91A>C
ENST00000680773.1:n.1089A>C
ENST00000680806.1:c.*1891A>C	ENSP00000506418.1:n.*1891A>C
ENST00000680997.1:n.520A>C
ENST00000681088.1:c.835A>C
ENST00000681608.1:n.121A>C
ENST00000681625.1:c.*505A>C	ENSP00000505555.1:n.*505A>C
ENST00000270301.11:c.3173A>C	ENSP00000270301.6:p.Lys1058Thr
ENST00000401500.6:c.3173A>C	ENSP00000384792.1:p.Lys1058Thr
ENST00000587391.5:c.*2448A>C	ENSP00000465525.1:n.*2448A>C
NM_001083961.1:c.3173A>C	NP_001077430.1:p.Lys1058Thr
NM_173636.4:c.3173A>C	NP_775907.4:p.Lys1058Thr
XM_005258809.2:c.3062A>C	XP_005258866.1:p.Lys1021Thr
XM_011526837.1:c.3158A>C	XP_011525139.1:p.Lys1053Thr
XM_011526838.1:c.2972-633A>C	XP_011525140.1:n.2972-633A>C
XM_011526839.1:c.2822A>C	XP_011525141.1:p.Lys941Thr
XM_011526840.1:c.2165A>C	XP_011525142.1:p.Lys722Thr
XM_011526841.1:c.1751A>C	XP_011525143.1:p.Lys584Thr
XM_011526842.1:c.1604A>C	XP_011525144.1:p.Lys535Thr
XM_011526843.1:c.920A>C	XP_011525145.1:p.Lys307Thr
XM_011526844.1:c.920A>C	XP_011525146.1:p.Lys307Thr
XM_011526840.2:c.2165A>C	XP_011525142.1:p.Lys722Thr
XM_011526841.2:c.1751A>C	XP_011525143.1:p.Lys584Thr
XM_011526844.2:c.920A>C	XP_011525146.1:p.Lys307Thr
XM_017026665.1:c.3173A>C	XP_016882154.1:p.Lys1058Thr
NM_001083961.2:c.3173A>C MANE Select	NP_001077430.1:p.Lys1058Thr
NM_173636.5:c.3173A>C	NP_775907.4:p.Lys1058Thr