Canonical Allele Identifier: CA405460959

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104612-G-C
• MyVariant Identifiers: chr19:g.36595514G>C (hg19) ; chr19:g.36104612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104612G>C , CM000681.2:g.36104612G>C	GRCh38
NC_000019.9:g.36595514G>C , CM000681.1:g.36595514G>C	GRCh37
NC_000019.8:g.41287354G>C	NCBI36
NG_028101.1:g.54732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4233G>C	ENSP00000270301.6:p.Arg1411Ser
ENST00000401500.7:c.4248G>C MANE Select	ENSP00000384792.1:p.Arg1416Ser
ENST00000587391.6:c.*4108G>C	ENSP00000465525.1:n.*4108G>C
ENST00000679357.1:c.2328G>C
ENST00000679598.1:c.993G>C
ENST00000679682.1:c.4233G>C	ENSP00000506226.1:p.Arg1411Ser
ENST00000679714.1:c.4242G>C	ENSP00000506627.1:p.Arg1414Ser
ENST00000679757.1:c.3897G>C	ENSP00000505158.1:p.Arg1299Ser
ENST00000679858.1:c.*3630G>C	ENSP00000505655.1:n.*3630G>C
ENST00000680211.1:c.849G>C	ENSP00000506102.1:p.Arg283Ser
ENST00000680280.1:n.1751G>C
ENST00000680349.1:n.2897G>C
ENST00000680403.1:c.4233G>C	ENSP00000505677.1:p.Arg1411Ser
ENST00000680564.1:c.3999G>C	ENSP00000505582.1:p.Arg1333Ser
ENST00000680590.1:c.*2628G>C	ENSP00000505350.1:n.*2628G>C
ENST00000680597.1:c.981G>C
ENST00000680739.1:c.1263G>C
ENST00000680773.1:n.2749G>C
ENST00000680806.1:c.*3551G>C	ENSP00000506418.1:n.*3551G>C
ENST00000680997.1:n.2180G>C
ENST00000681608.1:n.2093G>C
ENST00000681625.1:c.*1580G>C	ENSP00000505555.1:n.*1580G>C
ENST00000681648.1:n.2299G>C
ENST00000270301.11:c.4233G>C	ENSP00000270301.6:p.Arg1411Ser
ENST00000401500.6:c.4248G>C	ENSP00000384792.1:p.Arg1416Ser
ENST00000587391.5:c.*4108G>C	ENSP00000465525.1:n.*4108G>C
NM_001083961.1:c.4248G>C	NP_001077430.1:p.Arg1416Ser
NM_173636.4:c.4233G>C	NP_775907.4:p.Arg1411Ser
XM_005258809.2:c.4137G>C	XP_005258866.1:p.Arg1379Ser
XM_011526837.1:c.4233G>C	XP_011525139.1:p.Arg1411Ser
XM_011526838.1:c.3999G>C	XP_011525140.1:p.Arg1333Ser
XM_011526839.1:c.3897G>C	XP_011525141.1:p.Arg1299Ser
XM_011526840.1:c.3240G>C	XP_011525142.1:p.Arg1080Ser
XM_011526841.1:c.2826G>C	XP_011525143.1:p.Arg942Ser
XM_011526842.1:c.2679G>C	XP_011525144.1:p.Arg893Ser
XM_011526843.1:c.1995G>C	XP_011525145.1:p.Arg665Ser
XM_011526844.1:c.1995G>C	XP_011525146.1:p.Arg665Ser
XM_011526840.2:c.3240G>C	XP_011525142.1:p.Arg1080Ser
XM_011526841.2:c.2826G>C	XP_011525143.1:p.Arg942Ser
XM_011526844.2:c.1995G>C	XP_011525146.1:p.Arg665Ser
XM_017026665.1:c.4248G>C	XP_016882154.1:p.Arg1416Ser
NM_001083961.2:c.4248G>C MANE Select	NP_001077430.1:p.Arg1416Ser
NM_173636.5:c.4233G>C	NP_775907.4:p.Arg1411Ser