Canonical Allele Identifier: CA2584644423

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101967-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101967G>C , CM000681.2:g.36101967G>C	GRCh38
NC_000019.9:g.36592869G>C , CM000681.1:g.36592869G>C	GRCh37
NC_000019.8:g.41284709G>C	NCBI36
NG_028101.1:g.52087G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3083-47G>C	ENSP00000270301.6:n.3083-47G>C
ENST00000401500.7:c.3083-47G>C MANE Select	ENSP00000384792.1:n.3083-47G>C
ENST00000587391.6:c.*2311G>C	ENSP00000465525.1:n.*2311G>C
ENST00000679357.1:c.873-47G>C
ENST00000679422.1:c.762-47G>C
ENST00000679682.1:c.3068-47G>C	ENSP00000506226.1:n.3068-47G>C
ENST00000679714.1:c.3077-47G>C	ENSP00000506627.1:n.3077-47G>C
ENST00000679757.1:c.2732-47G>C	ENSP00000505158.1:n.2732-47G>C
ENST00000679858.1:c.*2418G>C	ENSP00000505655.1:n.*2418G>C
ENST00000680211.1:c.-317-47G>C	ENSP00000506102.1:n.-317-47G>C
ENST00000680349.1:n.1066-47G>C
ENST00000680403.1:c.3083-47G>C	ENSP00000505677.1:n.3083-47G>C
ENST00000680564.1:c.2971+650G>C	ENSP00000505582.1:n.2971+650G>C
ENST00000680590.1:c.*1478-47G>C	ENSP00000505350.1:n.*1478-47G>C
ENST00000680773.1:n.952G>C
ENST00000680806.1:c.*1801-47G>C	ENSP00000506418.1:n.*1801-47G>C
ENST00000680997.1:n.430-47G>C
ENST00000681088.1:c.745-47G>C
ENST00000681608.1:n.31-47G>C
ENST00000681625.1:c.*415-47G>C	ENSP00000505555.1:n.*415-47G>C
ENST00000270301.11:c.3083-47G>C	ENSP00000270301.6:n.3083-47G>C
ENST00000401500.6:c.3083-47G>C	ENSP00000384792.1:n.3083-47G>C
ENST00000587391.5:c.*2311G>C	ENSP00000465525.1:n.*2311G>C
NM_001083961.1:c.3083-47G>C	NP_001077430.1:n.3083-47G>C
NM_173636.4:c.3083-47G>C	NP_775907.4:n.3083-47G>C
XM_005258809.2:c.2972-47G>C	XP_005258866.1:n.2972-47G>C
XM_011526837.1:c.3068-47G>C	XP_011525139.1:n.3068-47G>C
XM_011526838.1:c.2971+650G>C	XP_011525140.1:n.2971+650G>C
XM_011526839.1:c.2732-47G>C	XP_011525141.1:n.2732-47G>C
XM_011526840.1:c.2075-47G>C	XP_011525142.1:n.2075-47G>C
XM_011526841.1:c.1661-47G>C	XP_011525143.1:n.1661-47G>C
XM_011526842.1:c.1514-47G>C	XP_011525144.1:n.1514-47G>C
XM_011526843.1:c.830-47G>C	XP_011525145.1:n.830-47G>C
XM_011526844.1:c.830-47G>C	XP_011525146.1:n.830-47G>C
XM_011526840.2:c.2075-47G>C	XP_011525142.1:n.2075-47G>C
XM_011526841.2:c.1661-47G>C	XP_011525143.1:n.1661-47G>C
XM_011526844.2:c.830-47G>C	XP_011525146.1:n.830-47G>C
XM_017026665.1:c.3083-47G>C	XP_016882154.1:n.3083-47G>C
NM_001083961.2:c.3083-47G>C MANE Select	NP_001077430.1:n.3083-47G>C
NM_173636.5:c.3083-47G>C	NP_775907.4:n.3083-47G>C