Canonical Allele Identifier: CA405461168

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595533A>G (hg19) ; chr19:g.36104631A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104631A>G , CM000681.2:g.36104631A>G	GRCh38
NC_000019.9:g.36595533A>G , CM000681.1:g.36595533A>G	GRCh37
NC_000019.8:g.41287373A>G	NCBI36
NG_028101.1:g.54751A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4252A>G	ENSP00000270301.6:p.Arg1418Gly
ENST00000401500.7:c.4267A>G MANE Select	ENSP00000384792.1:p.Arg1423Gly
ENST00000587391.6:c.*4127A>G	ENSP00000465525.1:n.*4127A>G
ENST00000679357.1:c.2347A>G
ENST00000679598.1:c.1012A>G
ENST00000679682.1:c.4252A>G	ENSP00000506226.1:p.Arg1418Gly
ENST00000679714.1:c.4261A>G	ENSP00000506627.1:p.Arg1421Gly
ENST00000679757.1:c.3916A>G	ENSP00000505158.1:p.Arg1306Gly
ENST00000679858.1:c.*3649A>G	ENSP00000505655.1:n.*3649A>G
ENST00000680211.1:c.868A>G	ENSP00000506102.1:p.Arg290Gly
ENST00000680280.1:n.1770A>G
ENST00000680349.1:n.2916A>G
ENST00000680403.1:c.4252A>G	ENSP00000505677.1:p.Arg1418Gly
ENST00000680564.1:c.4018A>G	ENSP00000505582.1:p.Arg1340Gly
ENST00000680590.1:c.*2647A>G	ENSP00000505350.1:n.*2647A>G
ENST00000680597.1:c.1000A>G
ENST00000680739.1:c.1282A>G
ENST00000680773.1:n.2768A>G
ENST00000680806.1:c.*3570A>G	ENSP00000506418.1:n.*3570A>G
ENST00000680997.1:n.2199A>G
ENST00000681608.1:n.2112A>G
ENST00000681625.1:c.*1599A>G	ENSP00000505555.1:n.*1599A>G
ENST00000681648.1:n.2318A>G
ENST00000270301.11:c.4252A>G	ENSP00000270301.6:p.Arg1418Gly
ENST00000401500.6:c.4267A>G	ENSP00000384792.1:p.Arg1423Gly
ENST00000587391.5:c.*4127A>G	ENSP00000465525.1:n.*4127A>G
NM_001083961.1:c.4267A>G	NP_001077430.1:p.Arg1423Gly
NM_173636.4:c.4252A>G	NP_775907.4:p.Arg1418Gly
XM_005258809.2:c.4156A>G	XP_005258866.1:p.Arg1386Gly
XM_011526837.1:c.4252A>G	XP_011525139.1:p.Arg1418Gly
XM_011526838.1:c.4018A>G	XP_011525140.1:p.Arg1340Gly
XM_011526839.1:c.3916A>G	XP_011525141.1:p.Arg1306Gly
XM_011526840.1:c.3259A>G	XP_011525142.1:p.Arg1087Gly
XM_011526841.1:c.2845A>G	XP_011525143.1:p.Arg949Gly
XM_011526842.1:c.2698A>G	XP_011525144.1:p.Arg900Gly
XM_011526843.1:c.2014A>G	XP_011525145.1:p.Arg672Gly
XM_011526844.1:c.2014A>G	XP_011525146.1:p.Arg672Gly
XM_011526840.2:c.3259A>G	XP_011525142.1:p.Arg1087Gly
XM_011526841.2:c.2845A>G	XP_011525143.1:p.Arg949Gly
XM_011526844.2:c.2014A>G	XP_011525146.1:p.Arg672Gly
XM_017026665.1:c.4267A>G	XP_016882154.1:p.Arg1423Gly
NM_001083961.2:c.4267A>G MANE Select	NP_001077430.1:p.Arg1423Gly
NM_173636.5:c.4252A>G	NP_775907.4:p.Arg1418Gly