Canonical Allele Identifier: CA405460600

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104568-G-T
• MyVariant Identifiers: chr19:g.36595470G>T (hg19) ; chr19:g.36104568G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104568G>T , CM000681.2:g.36104568G>T	GRCh38
NC_000019.9:g.36595470G>T , CM000681.1:g.36595470G>T	GRCh37
NC_000019.8:g.41287310G>T	NCBI36
NG_028101.1:g.54688G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4189G>T	ENSP00000270301.6:p.Val1397Leu
ENST00000401500.7:c.4204G>T MANE Select	ENSP00000384792.1:p.Val1402Leu
ENST00000587391.6:c.*4064G>T	ENSP00000465525.1:n.*4064G>T
ENST00000679357.1:c.2284G>T
ENST00000679598.1:c.949G>T
ENST00000679682.1:c.4189G>T	ENSP00000506226.1:p.Val1397Leu
ENST00000679714.1:c.4198G>T	ENSP00000506627.1:p.Val1400Leu
ENST00000679757.1:c.3853G>T	ENSP00000505158.1:p.Val1285Leu
ENST00000679858.1:c.*3586G>T	ENSP00000505655.1:n.*3586G>T
ENST00000680211.1:c.805G>T	ENSP00000506102.1:p.Val269Leu
ENST00000680280.1:n.1707G>T
ENST00000680349.1:n.2853G>T
ENST00000680403.1:c.4189G>T	ENSP00000505677.1:p.Val1397Leu
ENST00000680564.1:c.3955G>T	ENSP00000505582.1:p.Val1319Leu
ENST00000680590.1:c.*2584G>T	ENSP00000505350.1:n.*2584G>T
ENST00000680597.1:c.937G>T
ENST00000680739.1:c.1219G>T
ENST00000680773.1:n.2705G>T
ENST00000680806.1:c.*3507G>T	ENSP00000506418.1:n.*3507G>T
ENST00000680997.1:n.2136G>T
ENST00000681608.1:n.2049G>T
ENST00000681625.1:c.*1536G>T	ENSP00000505555.1:n.*1536G>T
ENST00000681648.1:n.2255G>T
ENST00000270301.11:c.4189G>T	ENSP00000270301.6:p.Val1397Leu
ENST00000401500.6:c.4204G>T	ENSP00000384792.1:p.Val1402Leu
ENST00000587391.5:c.*4064G>T	ENSP00000465525.1:n.*4064G>T
NM_001083961.1:c.4204G>T	NP_001077430.1:p.Val1402Leu
NM_173636.4:c.4189G>T	NP_775907.4:p.Val1397Leu
XM_005258809.2:c.4093G>T	XP_005258866.1:p.Val1365Leu
XM_011526837.1:c.4189G>T	XP_011525139.1:p.Val1397Leu
XM_011526838.1:c.3955G>T	XP_011525140.1:p.Val1319Leu
XM_011526839.1:c.3853G>T	XP_011525141.1:p.Val1285Leu
XM_011526840.1:c.3196G>T	XP_011525142.1:p.Val1066Leu
XM_011526841.1:c.2782G>T	XP_011525143.1:p.Val928Leu
XM_011526842.1:c.2635G>T	XP_011525144.1:p.Val879Leu
XM_011526843.1:c.1951G>T	XP_011525145.1:p.Val651Leu
XM_011526844.1:c.1951G>T	XP_011525146.1:p.Val651Leu
XM_011526840.2:c.3196G>T	XP_011525142.1:p.Val1066Leu
XM_011526841.2:c.2782G>T	XP_011525143.1:p.Val928Leu
XM_011526844.2:c.1951G>T	XP_011525146.1:p.Val651Leu
XM_017026665.1:c.4204G>T	XP_016882154.1:p.Val1402Leu
NM_001083961.2:c.4204G>T MANE Select	NP_001077430.1:p.Val1402Leu
NM_173636.5:c.4189G>T	NP_775907.4:p.Val1397Leu