Canonical Allele Identifier: CA405457501

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36594444G>T (hg19) ; chr19:g.36103542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103542G>T , CM000681.2:g.36103542G>T	GRCh38
NC_000019.9:g.36594444G>T , CM000681.1:g.36594444G>T	GRCh37
NC_000019.8:g.41286284G>T	NCBI36
NG_028101.1:g.53662G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3699G>T	ENSP00000270301.6:p.Glu1233Asp
ENST00000401500.7:c.3714G>T MANE Select	ENSP00000384792.1:p.Glu1238Asp
ENST00000587391.6:c.*3574G>T	ENSP00000465525.1:n.*3574G>T
ENST00000679357.1:c.1794G>T
ENST00000679598.1:c.479G>T
ENST00000679682.1:c.3699G>T	ENSP00000506226.1:p.Glu1233Asp
ENST00000679714.1:c.3708G>T	ENSP00000506627.1:p.Glu1236Asp
ENST00000679757.1:c.3363G>T	ENSP00000505158.1:p.Glu1121Asp
ENST00000679858.1:c.*3096G>T	ENSP00000505655.1:n.*3096G>T
ENST00000680211.1:c.315G>T	ENSP00000506102.1:p.Glu105Asp
ENST00000680280.1:n.1217G>T
ENST00000680349.1:n.2363G>T
ENST00000680403.1:c.3699G>T	ENSP00000505677.1:p.Glu1233Asp
ENST00000680564.1:c.3465G>T	ENSP00000505582.1:p.Glu1155Asp
ENST00000680590.1:c.*2094G>T	ENSP00000505350.1:n.*2094G>T
ENST00000680597.1:c.447G>T
ENST00000680739.1:c.729G>T
ENST00000680773.1:n.2215G>T
ENST00000680806.1:c.*3017G>T	ENSP00000506418.1:n.*3017G>T
ENST00000680997.1:n.1646G>T
ENST00000681608.1:n.1559G>T
ENST00000681625.1:c.*1046G>T	ENSP00000505555.1:n.*1046G>T
ENST00000681648.1:n.1229G>T
ENST00000270301.11:c.3699G>T	ENSP00000270301.6:p.Glu1233Asp
ENST00000401500.6:c.3714G>T	ENSP00000384792.1:p.Glu1238Asp
ENST00000587391.5:c.*3574G>T	ENSP00000465525.1:n.*3574G>T
NM_001083961.1:c.3714G>T	NP_001077430.1:p.Glu1238Asp
NM_173636.4:c.3699G>T	NP_775907.4:p.Glu1233Asp
XM_005258809.2:c.3603G>T	XP_005258866.1:p.Glu1201Asp
XM_011526837.1:c.3699G>T	XP_011525139.1:p.Glu1233Asp
XM_011526838.1:c.3465G>T	XP_011525140.1:p.Glu1155Asp
XM_011526839.1:c.3363G>T	XP_011525141.1:p.Glu1121Asp
XM_011526840.1:c.2706G>T	XP_011525142.1:p.Glu902Asp
XM_011526841.1:c.2292G>T	XP_011525143.1:p.Glu764Asp
XM_011526842.1:c.2145G>T	XP_011525144.1:p.Glu715Asp
XM_011526843.1:c.1461G>T	XP_011525145.1:p.Glu487Asp
XM_011526844.1:c.1461G>T	XP_011525146.1:p.Glu487Asp
XM_011526840.2:c.2706G>T	XP_011525142.1:p.Glu902Asp
XM_011526841.2:c.2292G>T	XP_011525143.1:p.Glu764Asp
XM_011526844.2:c.1461G>T	XP_011525146.1:p.Glu487Asp
XM_017026665.1:c.3714G>T	XP_016882154.1:p.Glu1238Asp
NM_001083961.2:c.3714G>T MANE Select	NP_001077430.1:p.Glu1238Asp
NM_173636.5:c.3699G>T	NP_775907.4:p.Glu1233Asp