Canonical Allele Identifier: CA405460741

Gene: WDR62

Linked Data

• dbSNP Id: rs2145886798
• gnomAD v4: 19-36104586-C-T
• COSMIC: COSM1393044
• MyVariant Identifiers: chr19:g.36595488C>T (hg19) ; chr19:g.36104586C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104586C>T , CM000681.2:g.36104586C>T	GRCh38
NC_000019.9:g.36595488C>T , CM000681.1:g.36595488C>T	GRCh37
NC_000019.8:g.41287328C>T	NCBI36
NG_028101.1:g.54706C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4207C>T	ENSP00000270301.6:p.Pro1403Ser
ENST00000401500.7:c.4222C>T MANE Select	ENSP00000384792.1:p.Pro1408Ser
ENST00000587391.6:c.*4082C>T	ENSP00000465525.1:n.*4082C>T
ENST00000679357.1:c.2302C>T
ENST00000679598.1:c.967C>T
ENST00000679682.1:c.4207C>T	ENSP00000506226.1:p.Pro1403Ser
ENST00000679714.1:c.4216C>T	ENSP00000506627.1:p.Pro1406Ser
ENST00000679757.1:c.3871C>T	ENSP00000505158.1:p.Pro1291Ser
ENST00000679858.1:c.*3604C>T	ENSP00000505655.1:n.*3604C>T
ENST00000680211.1:c.823C>T	ENSP00000506102.1:p.Pro275Ser
ENST00000680280.1:n.1725C>T
ENST00000680349.1:n.2871C>T
ENST00000680403.1:c.4207C>T	ENSP00000505677.1:p.Pro1403Ser
ENST00000680564.1:c.3973C>T	ENSP00000505582.1:p.Pro1325Ser
ENST00000680590.1:c.*2602C>T	ENSP00000505350.1:n.*2602C>T
ENST00000680597.1:c.955C>T
ENST00000680739.1:c.1237C>T
ENST00000680773.1:n.2723C>T
ENST00000680806.1:c.*3525C>T	ENSP00000506418.1:n.*3525C>T
ENST00000680997.1:n.2154C>T
ENST00000681608.1:n.2067C>T
ENST00000681625.1:c.*1554C>T	ENSP00000505555.1:n.*1554C>T
ENST00000681648.1:n.2273C>T
ENST00000270301.11:c.4207C>T	ENSP00000270301.6:p.Pro1403Ser
ENST00000401500.6:c.4222C>T	ENSP00000384792.1:p.Pro1408Ser
ENST00000587391.5:c.*4082C>T	ENSP00000465525.1:n.*4082C>T
NM_001083961.1:c.4222C>T	NP_001077430.1:p.Pro1408Ser
NM_173636.4:c.4207C>T	NP_775907.4:p.Pro1403Ser
XM_005258809.2:c.4111C>T	XP_005258866.1:p.Pro1371Ser
XM_011526837.1:c.4207C>T	XP_011525139.1:p.Pro1403Ser
XM_011526838.1:c.3973C>T	XP_011525140.1:p.Pro1325Ser
XM_011526839.1:c.3871C>T	XP_011525141.1:p.Pro1291Ser
XM_011526840.1:c.3214C>T	XP_011525142.1:p.Pro1072Ser
XM_011526841.1:c.2800C>T	XP_011525143.1:p.Pro934Ser
XM_011526842.1:c.2653C>T	XP_011525144.1:p.Pro885Ser
XM_011526843.1:c.1969C>T	XP_011525145.1:p.Pro657Ser
XM_011526844.1:c.1969C>T	XP_011525146.1:p.Pro657Ser
XM_011526840.2:c.3214C>T	XP_011525142.1:p.Pro1072Ser
XM_011526841.2:c.2800C>T	XP_011525143.1:p.Pro934Ser
XM_011526844.2:c.1969C>T	XP_011525146.1:p.Pro657Ser
XM_017026665.1:c.4222C>T	XP_016882154.1:p.Pro1408Ser
NM_001083961.2:c.4222C>T MANE Select	NP_001077430.1:p.Pro1408Ser
NM_173636.5:c.4207C>T	NP_775907.4:p.Pro1403Ser