Canonical Allele Identifier: CA405437360

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36574073G>C (hg19) ; chr19:g.36083171G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36083171G>C , CM000681.2:g.36083171G>C	GRCh38
NC_000019.9:g.36574073G>C , CM000681.1:g.36574073G>C	GRCh37
NC_000019.8:g.41265913G>C	NCBI36
NG_028101.1:g.33291G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.1480G>C	ENSP00000270301.6:p.Gly494Arg
ENST00000401500.7:c.1480G>C MANE Select	ENSP00000384792.1:p.Gly494Arg
ENST00000587391.6:c.*170G>C	ENSP00000465525.1:n.*170G>C
ENST00000644764.2:c.*272G>C	ENSP00000494253.2:n.*272G>C
ENST00000679682.1:c.1465G>C	ENSP00000506226.1:p.Gly489Arg
ENST00000679714.1:c.1474G>C	ENSP00000506627.1:p.Gly492Arg
ENST00000679757.1:c.1129G>C	ENSP00000505158.1:p.Gly377Arg
ENST00000679858.1:c.*277G>C	ENSP00000505655.1:n.*277G>C
ENST00000680359.1:c.1480G>C	ENSP00000506079.1:p.Gly494Arg
ENST00000680403.1:c.1480G>C	ENSP00000505677.1:p.Gly494Arg
ENST00000680489.1:n.1803G>C
ENST00000680564.1:c.1480G>C	ENSP00000505582.1:p.Gly494Arg
ENST00000680590.1:c.1480G>C	ENSP00000505350.1:p.Gly494Arg
ENST00000680806.1:c.*309G>C	ENSP00000506418.1:n.*309G>C
ENST00000681625.1:c.1465G>C	ENSP00000505555.1:p.Gly489Arg
ENST00000270301.11:c.1480G>C	ENSP00000270301.6:p.Gly494Arg
ENST00000401500.6:c.1480G>C	ENSP00000384792.1:p.Gly494Arg
ENST00000587391.5:c.*170G>C	ENSP00000465525.1:n.*170G>C
NM_001083961.1:c.1480G>C	NP_001077430.1:p.Gly494Arg
NM_173636.4:c.1480G>C	NP_775907.4:p.Gly494Arg
XM_005258809.2:c.1480G>C	XP_005258866.1:p.Gly494Arg
XM_011526837.1:c.1465G>C	XP_011525139.1:p.Gly489Arg
XM_011526838.1:c.1480G>C	XP_011525140.1:p.Gly494Arg
XM_011526839.1:c.1129G>C	XP_011525141.1:p.Gly377Arg
XM_011526840.1:c.472G>C	XP_011525142.1:p.Gly158Arg
XM_011526841.1:c.58G>C	XP_011525143.1:p.Gly20Arg
XM_011526842.1:c.-37G>C	XP_011525144.1:n.-37G>C
XM_011526840.2:c.472G>C	XP_011525142.1:p.Gly158Arg
XM_011526841.2:c.58G>C	XP_011525143.1:p.Gly20Arg
XM_017026665.1:c.1480G>C	XP_016882154.1:p.Gly494Arg
XR_001753671.1:n.1571G>C
XR_001753672.1:n.1571G>C
NM_001083961.2:c.1480G>C MANE Select	NP_001077430.1:p.Gly494Arg
NM_173636.5:c.1480G>C	NP_775907.4:p.Gly494Arg