Canonical Allele Identifier: CA405450963

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102152-G-A
• MyVariant Identifiers: chr19:g.36593054G>A (hg19) ; chr19:g.36102152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102152G>A , CM000681.2:g.36102152G>A	GRCh38
NC_000019.9:g.36593054G>A , CM000681.1:g.36593054G>A	GRCh37
NC_000019.8:g.41284894G>A	NCBI36
NG_028101.1:g.52272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3220+1G>A	ENSP00000270301.6:n.3220+1G>A
ENST00000401500.7:c.3220+1G>A MANE Select	ENSP00000384792.1:n.3220+1G>A
ENST00000587391.6:c.*2496G>A	ENSP00000465525.1:n.*2496G>A
ENST00000679357.1:c.1010+1G>A
ENST00000679682.1:c.3205+1G>A	ENSP00000506226.1:n.3205+1G>A
ENST00000679714.1:c.3214+1G>A	ENSP00000506627.1:n.3214+1G>A
ENST00000679757.1:c.2869+1G>A	ENSP00000505158.1:n.2869+1G>A
ENST00000679858.1:c.*2602+1G>A	ENSP00000505655.1:n.*2602+1G>A
ENST00000680211.1:c.-180+1G>A	ENSP00000506102.1:n.-180+1G>A
ENST00000680349.1:n.1204G>A
ENST00000680403.1:c.3220+1G>A	ENSP00000505677.1:n.3220+1G>A
ENST00000680564.1:c.2972-585G>A	ENSP00000505582.1:n.2972-585G>A
ENST00000680590.1:c.*1615+1G>A	ENSP00000505350.1:n.*1615+1G>A
ENST00000680739.1:c.139G>A
ENST00000680773.1:n.1137G>A
ENST00000680806.1:c.*1939G>A	ENSP00000506418.1:n.*1939G>A
ENST00000680997.1:n.568G>A
ENST00000681608.1:n.169G>A
ENST00000681625.1:c.*552+1G>A	ENSP00000505555.1:n.*552+1G>A
ENST00000270301.11:c.3220+1G>A	ENSP00000270301.6:n.3220+1G>A
ENST00000401500.6:c.3220+1G>A	ENSP00000384792.1:n.3220+1G>A
ENST00000587391.5:c.*2496G>A	ENSP00000465525.1:n.*2496G>A
NM_001083961.1:c.3220+1G>A	NP_001077430.1:n.3220+1G>A
NM_173636.4:c.3220+1G>A	NP_775907.4:n.3220+1G>A
XM_005258809.2:c.3109+1G>A	XP_005258866.1:n.3109+1G>A
XM_011526837.1:c.3205+1G>A	XP_011525139.1:n.3205+1G>A
XM_011526838.1:c.2972-585G>A	XP_011525140.1:n.2972-585G>A
XM_011526839.1:c.2869+1G>A	XP_011525141.1:n.2869+1G>A
XM_011526840.1:c.2212+1G>A	XP_011525142.1:n.2212+1G>A
XM_011526841.1:c.1798+1G>A	XP_011525143.1:n.1798+1G>A
XM_011526842.1:c.1651+1G>A	XP_011525144.1:n.1651+1G>A
XM_011526843.1:c.967+1G>A	XP_011525145.1:n.967+1G>A
XM_011526844.1:c.967+1G>A	XP_011525146.1:n.967+1G>A
XM_011526840.2:c.2212+1G>A	XP_011525142.1:n.2212+1G>A
XM_011526841.2:c.1798+1G>A	XP_011525143.1:n.1798+1G>A
XM_011526844.2:c.967+1G>A	XP_011525146.1:n.967+1G>A
XM_017026665.1:c.3220+1G>A	XP_016882154.1:n.3220+1G>A
NM_001083961.2:c.3220+1G>A MANE Select	NP_001077430.1:n.3220+1G>A
NM_173636.5:c.3220+1G>A	NP_775907.4:n.3220+1G>A