Canonical Allele Identifier: CA507318719

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595526C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104624C>T , CM000681.2:g.36104624C>T	GRCh38
NC_000019.9:g.36595526C>T , CM000681.1:g.36595526C>T	GRCh37
NC_000019.8:g.41287366C>T	NCBI36
NG_028101.1:g.54744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4245C>T	ENSP00000270301.6:p.Ile1415=
ENST00000401500.7:c.4260C>T MANE Select	ENSP00000384792.1:p.Ile1420=
ENST00000587391.6:c.*4120C>T	ENSP00000465525.1:n.*4120C>T
ENST00000679357.1:c.2340C>T
ENST00000679598.1:c.1005C>T
ENST00000679682.1:c.4245C>T	ENSP00000506226.1:p.Ile1415=
ENST00000679714.1:c.4254C>T	ENSP00000506627.1:p.Ile1418=
ENST00000679757.1:c.3909C>T	ENSP00000505158.1:p.Ile1303=
ENST00000679858.1:c.*3642C>T	ENSP00000505655.1:n.*3642C>T
ENST00000680211.1:c.861C>T	ENSP00000506102.1:p.Ile287=
ENST00000680280.1:n.1763C>T
ENST00000680349.1:n.2909C>T
ENST00000680403.1:c.4245C>T	ENSP00000505677.1:p.Ile1415=
ENST00000680564.1:c.4011C>T	ENSP00000505582.1:p.Ile1337=
ENST00000680590.1:c.*2640C>T	ENSP00000505350.1:n.*2640C>T
ENST00000680597.1:c.993C>T
ENST00000680739.1:c.1275C>T
ENST00000680773.1:n.2761C>T
ENST00000680806.1:c.*3563C>T	ENSP00000506418.1:n.*3563C>T
ENST00000680997.1:n.2192C>T
ENST00000681608.1:n.2105C>T
ENST00000681625.1:c.*1592C>T	ENSP00000505555.1:n.*1592C>T
ENST00000681648.1:n.2311C>T
ENST00000270301.11:c.4245C>T	ENSP00000270301.6:p.Ile1415=
ENST00000401500.6:c.4260C>T	ENSP00000384792.1:p.Ile1420=
ENST00000587391.5:c.*4120C>T	ENSP00000465525.1:n.*4120C>T
NM_001083961.1:c.4260C>T	NP_001077430.1:p.Ile1420=
NM_173636.4:c.4245C>T	NP_775907.4:p.Ile1415=
XM_005258809.2:c.4149C>T	XP_005258866.1:p.Ile1383=
XM_011526837.1:c.4245C>T	XP_011525139.1:p.Ile1415=
XM_011526838.1:c.4011C>T	XP_011525140.1:p.Ile1337=
XM_011526839.1:c.3909C>T	XP_011525141.1:p.Ile1303=
XM_011526840.1:c.3252C>T	XP_011525142.1:p.Ile1084=
XM_011526841.1:c.2838C>T	XP_011525143.1:p.Ile946=
XM_011526842.1:c.2691C>T	XP_011525144.1:p.Ile897=
XM_011526843.1:c.2007C>T	XP_011525145.1:p.Ile669=
XM_011526844.1:c.2007C>T	XP_011525146.1:p.Ile669=
XM_011526840.2:c.3252C>T	XP_011525142.1:p.Ile1084=
XM_011526841.2:c.2838C>T	XP_011525143.1:p.Ile946=
XM_011526844.2:c.2007C>T	XP_011525146.1:p.Ile669=
XM_017026665.1:c.4260C>T	XP_016882154.1:p.Ile1420=
NM_001083961.2:c.4260C>T MANE Select	NP_001077430.1:p.Ile1420=
NM_173636.5:c.4245C>T	NP_775907.4:p.Ile1415=