Canonical Allele Identifier: CA405460472

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595459G>C (hg19) ; chr19:g.36104557G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104557G>C , CM000681.2:g.36104557G>C	GRCh38
NC_000019.9:g.36595459G>C , CM000681.1:g.36595459G>C	GRCh37
NC_000019.8:g.41287299G>C	NCBI36
NG_028101.1:g.54677G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4178G>C	ENSP00000270301.6:p.Ser1393Thr
ENST00000401500.7:c.4193G>C MANE Select	ENSP00000384792.1:p.Ser1398Thr
ENST00000587391.6:c.*4053G>C	ENSP00000465525.1:n.*4053G>C
ENST00000679357.1:c.2273G>C
ENST00000679598.1:c.938G>C
ENST00000679682.1:c.4178G>C	ENSP00000506226.1:p.Ser1393Thr
ENST00000679714.1:c.4187G>C	ENSP00000506627.1:p.Ser1396Thr
ENST00000679757.1:c.3842G>C	ENSP00000505158.1:p.Ser1281Thr
ENST00000679858.1:c.*3575G>C	ENSP00000505655.1:n.*3575G>C
ENST00000680211.1:c.794G>C	ENSP00000506102.1:p.Ser265Thr
ENST00000680280.1:n.1696G>C
ENST00000680349.1:n.2842G>C
ENST00000680403.1:c.4178G>C	ENSP00000505677.1:p.Ser1393Thr
ENST00000680564.1:c.3944G>C	ENSP00000505582.1:p.Ser1315Thr
ENST00000680590.1:c.*2573G>C	ENSP00000505350.1:n.*2573G>C
ENST00000680597.1:c.926G>C
ENST00000680739.1:c.1208G>C
ENST00000680773.1:n.2694G>C
ENST00000680806.1:c.*3496G>C	ENSP00000506418.1:n.*3496G>C
ENST00000680997.1:n.2125G>C
ENST00000681608.1:n.2038G>C
ENST00000681625.1:c.*1525G>C	ENSP00000505555.1:n.*1525G>C
ENST00000681648.1:n.2244G>C
ENST00000270301.11:c.4178G>C	ENSP00000270301.6:p.Ser1393Thr
ENST00000401500.6:c.4193G>C	ENSP00000384792.1:p.Ser1398Thr
ENST00000587391.5:c.*4053G>C	ENSP00000465525.1:n.*4053G>C
NM_001083961.1:c.4193G>C	NP_001077430.1:p.Ser1398Thr
NM_173636.4:c.4178G>C	NP_775907.4:p.Ser1393Thr
XM_005258809.2:c.4082G>C	XP_005258866.1:p.Ser1361Thr
XM_011526837.1:c.4178G>C	XP_011525139.1:p.Ser1393Thr
XM_011526838.1:c.3944G>C	XP_011525140.1:p.Ser1315Thr
XM_011526839.1:c.3842G>C	XP_011525141.1:p.Ser1281Thr
XM_011526840.1:c.3185G>C	XP_011525142.1:p.Ser1062Thr
XM_011526841.1:c.2771G>C	XP_011525143.1:p.Ser924Thr
XM_011526842.1:c.2624G>C	XP_011525144.1:p.Ser875Thr
XM_011526843.1:c.1940G>C	XP_011525145.1:p.Ser647Thr
XM_011526844.1:c.1940G>C	XP_011525146.1:p.Ser647Thr
XM_011526840.2:c.3185G>C	XP_011525142.1:p.Ser1062Thr
XM_011526841.2:c.2771G>C	XP_011525143.1:p.Ser924Thr
XM_011526844.2:c.1940G>C	XP_011525146.1:p.Ser647Thr
XM_017026665.1:c.4193G>C	XP_016882154.1:p.Ser1398Thr
NM_001083961.2:c.4193G>C MANE Select	NP_001077430.1:p.Ser1398Thr
NM_173636.5:c.4178G>C	NP_775907.4:p.Ser1393Thr