Canonical Allele Identifier: CA2739276656

Gene: WDR62

Linked Data

• ClinVar Variation Id: 2810127
• ClinVar RCV Id: RCV003680298

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102160C>G , CM000681.2:g.36102160C>G	GRCh38
NC_000019.9:g.36593062C>G , CM000681.1:g.36593062C>G	GRCh37
NC_000019.8:g.41284902C>G	NCBI36
NG_028101.1:g.52280C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3220+9C>G	ENSP00000270301.6:n.3220+9C>G
ENST00000401500.7:c.3220+9C>G MANE Select	ENSP00000384792.1:n.3220+9C>G
ENST00000587391.6:c.*2504C>G	ENSP00000465525.1:n.*2504C>G
ENST00000679357.1:c.1010+9C>G
ENST00000679682.1:c.3205+9C>G	ENSP00000506226.1:n.3205+9C>G
ENST00000679714.1:c.3214+9C>G	ENSP00000506627.1:n.3214+9C>G
ENST00000679757.1:c.2869+9C>G	ENSP00000505158.1:n.2869+9C>G
ENST00000679858.1:c.*2602+9C>G	ENSP00000505655.1:n.*2602+9C>G
ENST00000680211.1:c.-180+9C>G	ENSP00000506102.1:n.-180+9C>G
ENST00000680349.1:n.1212C>G
ENST00000680403.1:c.3220+9C>G	ENSP00000505677.1:n.3220+9C>G
ENST00000680564.1:c.2972-577C>G	ENSP00000505582.1:n.2972-577C>G
ENST00000680590.1:c.*1615+9C>G	ENSP00000505350.1:n.*1615+9C>G
ENST00000680739.1:c.147C>G
ENST00000680773.1:n.1145C>G
ENST00000680806.1:c.*1947C>G	ENSP00000506418.1:n.*1947C>G
ENST00000680997.1:n.576C>G
ENST00000681608.1:n.177C>G
ENST00000681625.1:c.*552+9C>G	ENSP00000505555.1:n.*552+9C>G
ENST00000270301.11:c.3220+9C>G	ENSP00000270301.6:n.3220+9C>G
ENST00000401500.6:c.3220+9C>G	ENSP00000384792.1:n.3220+9C>G
ENST00000587391.5:c.*2504C>G	ENSP00000465525.1:n.*2504C>G
NM_001083961.1:c.3220+9C>G	NP_001077430.1:n.3220+9C>G
NM_173636.4:c.3220+9C>G	NP_775907.4:n.3220+9C>G
XM_005258809.2:c.3109+9C>G	XP_005258866.1:n.3109+9C>G
XM_011526837.1:c.3205+9C>G	XP_011525139.1:n.3205+9C>G
XM_011526838.1:c.2972-577C>G	XP_011525140.1:n.2972-577C>G
XM_011526839.1:c.2869+9C>G	XP_011525141.1:n.2869+9C>G
XM_011526840.1:c.2212+9C>G	XP_011525142.1:n.2212+9C>G
XM_011526841.1:c.1798+9C>G	XP_011525143.1:n.1798+9C>G
XM_011526842.1:c.1651+9C>G	XP_011525144.1:n.1651+9C>G
XM_011526843.1:c.967+9C>G	XP_011525145.1:n.967+9C>G
XM_011526844.1:c.967+9C>G	XP_011525146.1:n.967+9C>G
XM_011526840.2:c.2212+9C>G	XP_011525142.1:n.2212+9C>G
XM_011526841.2:c.1798+9C>G	XP_011525143.1:n.1798+9C>G
XM_011526844.2:c.967+9C>G	XP_011525146.1:n.967+9C>G
XM_017026665.1:c.3220+9C>G	XP_016882154.1:n.3220+9C>G
NM_001083961.2:c.3220+9C>G MANE Select	NP_001077430.1:n.3220+9C>G
NM_173636.5:c.3220+9C>G	NP_775907.4:n.3220+9C>G