Canonical Allele Identifier: CA405451898

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593699A>C (hg19) ; chr19:g.36102797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102797A>C , CM000681.2:g.36102797A>C	GRCh38
NC_000019.9:g.36593699A>C , CM000681.1:g.36593699A>C	GRCh37
NC_000019.8:g.41285539A>C	NCBI36
NG_028101.1:g.52917A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3266A>C	ENSP00000270301.6:p.Asn1089Thr
ENST00000401500.7:c.3281A>C MANE Select	ENSP00000384792.1:p.Asn1094Thr
ENST00000587391.6:c.*3141A>C	ENSP00000465525.1:n.*3141A>C
ENST00000679357.1:c.1361A>C
ENST00000679598.1:c.46A>C
ENST00000679682.1:c.3266A>C	ENSP00000506226.1:p.Asn1089Thr
ENST00000679714.1:c.3275A>C	ENSP00000506627.1:p.Asn1092Thr
ENST00000679757.1:c.2930A>C	ENSP00000505158.1:p.Asn977Thr
ENST00000679858.1:c.*2663A>C	ENSP00000505655.1:n.*2663A>C
ENST00000680211.1:c.-119A>C	ENSP00000506102.1:n.-119A>C
ENST00000680280.1:n.568A>C
ENST00000680349.1:n.1849A>C
ENST00000680403.1:c.3266A>C	ENSP00000505677.1:p.Asn1089Thr
ENST00000680564.1:c.3032A>C	ENSP00000505582.1:p.Asn1011Thr
ENST00000680590.1:c.*1661A>C	ENSP00000505350.1:n.*1661A>C
ENST00000680597.1:c.46A>C
ENST00000680739.1:c.296A>C
ENST00000680773.1:n.1782A>C
ENST00000680806.1:c.*2584A>C	ENSP00000506418.1:n.*2584A>C
ENST00000680997.1:n.1213A>C
ENST00000681608.1:n.814A>C
ENST00000681625.1:c.*613A>C	ENSP00000505555.1:n.*613A>C
ENST00000681648.1:n.580A>C
ENST00000270301.11:c.3266A>C	ENSP00000270301.6:p.Asn1089Thr
ENST00000401500.6:c.3281A>C	ENSP00000384792.1:p.Asn1094Thr
ENST00000587391.5:c.*3141A>C	ENSP00000465525.1:n.*3141A>C
NM_001083961.1:c.3281A>C	NP_001077430.1:p.Asn1094Thr
NM_173636.4:c.3266A>C	NP_775907.4:p.Asn1089Thr
XM_005258809.2:c.3170A>C	XP_005258866.1:p.Asn1057Thr
XM_011526837.1:c.3266A>C	XP_011525139.1:p.Asn1089Thr
XM_011526838.1:c.3032A>C	XP_011525140.1:p.Asn1011Thr
XM_011526839.1:c.2930A>C	XP_011525141.1:p.Asn977Thr
XM_011526840.1:c.2273A>C	XP_011525142.1:p.Asn758Thr
XM_011526841.1:c.1859A>C	XP_011525143.1:p.Asn620Thr
XM_011526842.1:c.1712A>C	XP_011525144.1:p.Asn571Thr
XM_011526843.1:c.1028A>C	XP_011525145.1:p.Asn343Thr
XM_011526844.1:c.1028A>C	XP_011525146.1:p.Asn343Thr
XM_011526840.2:c.2273A>C	XP_011525142.1:p.Asn758Thr
XM_011526841.2:c.1859A>C	XP_011525143.1:p.Asn620Thr
XM_011526844.2:c.1028A>C	XP_011525146.1:p.Asn343Thr
XM_017026665.1:c.3281A>C	XP_016882154.1:p.Asn1094Thr
NM_001083961.2:c.3281A>C MANE Select	NP_001077430.1:p.Asn1094Thr
NM_173636.5:c.3266A>C	NP_775907.4:p.Asn1089Thr