Canonical Allele Identifier: CA405460272

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595422G>T (hg19) ; chr19:g.36104520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104520G>T , CM000681.2:g.36104520G>T	GRCh38
NC_000019.9:g.36595422G>T , CM000681.1:g.36595422G>T	GRCh37
NC_000019.8:g.41287262G>T	NCBI36
NG_028101.1:g.54640G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4141G>T	ENSP00000270301.6:p.Ala1381Ser
ENST00000401500.7:c.4156G>T MANE Select	ENSP00000384792.1:p.Ala1386Ser
ENST00000587391.6:c.*4016G>T	ENSP00000465525.1:n.*4016G>T
ENST00000679357.1:c.2236G>T
ENST00000679598.1:c.919-18G>T
ENST00000679682.1:c.4141G>T	ENSP00000506226.1:p.Ala1381Ser
ENST00000679714.1:c.4150G>T	ENSP00000506627.1:p.Ala1384Ser
ENST00000679757.1:c.3805G>T	ENSP00000505158.1:p.Ala1269Ser
ENST00000679858.1:c.*3538G>T	ENSP00000505655.1:n.*3538G>T
ENST00000680211.1:c.757G>T	ENSP00000506102.1:p.Ala253Ser
ENST00000680280.1:n.1659G>T
ENST00000680349.1:n.2805G>T
ENST00000680403.1:c.4141G>T	ENSP00000505677.1:p.Ala1381Ser
ENST00000680564.1:c.3907G>T	ENSP00000505582.1:p.Ala1303Ser
ENST00000680590.1:c.*2536G>T	ENSP00000505350.1:n.*2536G>T
ENST00000680597.1:c.889G>T
ENST00000680739.1:c.1171G>T
ENST00000680773.1:n.2657G>T
ENST00000680806.1:c.*3459G>T	ENSP00000506418.1:n.*3459G>T
ENST00000680997.1:n.2088G>T
ENST00000681608.1:n.2001G>T
ENST00000681625.1:c.*1488G>T	ENSP00000505555.1:n.*1488G>T
ENST00000681648.1:n.2207G>T
ENST00000270301.11:c.4141G>T	ENSP00000270301.6:p.Ala1381Ser
ENST00000401500.6:c.4156G>T	ENSP00000384792.1:p.Ala1386Ser
ENST00000587391.5:c.*4016G>T	ENSP00000465525.1:n.*4016G>T
NM_001083961.1:c.4156G>T	NP_001077430.1:p.Ala1386Ser
NM_173636.4:c.4141G>T	NP_775907.4:p.Ala1381Ser
XM_005258809.2:c.4045G>T	XP_005258866.1:p.Ala1349Ser
XM_011526837.1:c.4141G>T	XP_011525139.1:p.Ala1381Ser
XM_011526838.1:c.3907G>T	XP_011525140.1:p.Ala1303Ser
XM_011526839.1:c.3805G>T	XP_011525141.1:p.Ala1269Ser
XM_011526840.1:c.3148G>T	XP_011525142.1:p.Ala1050Ser
XM_011526841.1:c.2734G>T	XP_011525143.1:p.Ala912Ser
XM_011526842.1:c.2587G>T	XP_011525144.1:p.Ala863Ser
XM_011526843.1:c.1903G>T	XP_011525145.1:p.Ala635Ser
XM_011526844.1:c.1903G>T	XP_011525146.1:p.Ala635Ser
XM_011526840.2:c.3148G>T	XP_011525142.1:p.Ala1050Ser
XM_011526841.2:c.2734G>T	XP_011525143.1:p.Ala912Ser
XM_011526844.2:c.1903G>T	XP_011525146.1:p.Ala635Ser
XM_017026665.1:c.4156G>T	XP_016882154.1:p.Ala1386Ser
NM_001083961.2:c.4156G>T MANE Select	NP_001077430.1:p.Ala1386Ser
NM_173636.5:c.4141G>T	NP_775907.4:p.Ala1381Ser