Canonical Allele Identifier: CA405450943

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593051G>T (hg19) ; chr19:g.36102149G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102149G>T , CM000681.2:g.36102149G>T	GRCh38
NC_000019.9:g.36593051G>T , CM000681.1:g.36593051G>T	GRCh37
NC_000019.8:g.41284891G>T	NCBI36
NG_028101.1:g.52269G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3218G>T	ENSP00000270301.6:p.Arg1073Ile
ENST00000401500.7:c.3218G>T MANE Select	ENSP00000384792.1:p.Arg1073Ile
ENST00000587391.6:c.*2493G>T	ENSP00000465525.1:n.*2493G>T
ENST00000679357.1:c.1008G>T
ENST00000679422.1:c.897G>T
ENST00000679682.1:c.3203G>T	ENSP00000506226.1:p.Arg1068Ile
ENST00000679714.1:c.3212G>T	ENSP00000506627.1:p.Arg1071Ile
ENST00000679757.1:c.2867G>T	ENSP00000505158.1:p.Arg956Ile
ENST00000679858.1:c.*2600G>T	ENSP00000505655.1:n.*2600G>T
ENST00000680211.1:c.-182G>T	ENSP00000506102.1:n.-182G>T
ENST00000680349.1:n.1201G>T
ENST00000680403.1:c.3218G>T	ENSP00000505677.1:p.Arg1073Ile
ENST00000680564.1:c.2972-588G>T	ENSP00000505582.1:n.2972-588G>T
ENST00000680590.1:c.*1613G>T	ENSP00000505350.1:n.*1613G>T
ENST00000680739.1:c.136G>T
ENST00000680773.1:n.1134G>T
ENST00000680806.1:c.*1936G>T	ENSP00000506418.1:n.*1936G>T
ENST00000680997.1:n.565G>T
ENST00000681088.1:c.880G>T
ENST00000681608.1:n.166G>T
ENST00000681625.1:c.*550G>T	ENSP00000505555.1:n.*550G>T
ENST00000270301.11:c.3218G>T	ENSP00000270301.6:p.Arg1073Ile
ENST00000401500.6:c.3218G>T	ENSP00000384792.1:p.Arg1073Ile
ENST00000587391.5:c.*2493G>T	ENSP00000465525.1:n.*2493G>T
NM_001083961.1:c.3218G>T	NP_001077430.1:p.Arg1073Ile
NM_173636.4:c.3218G>T	NP_775907.4:p.Arg1073Ile
XM_005258809.2:c.3107G>T	XP_005258866.1:p.Arg1036Ile
XM_011526837.1:c.3203G>T	XP_011525139.1:p.Arg1068Ile
XM_011526838.1:c.2972-588G>T	XP_011525140.1:n.2972-588G>T
XM_011526839.1:c.2867G>T	XP_011525141.1:p.Arg956Ile
XM_011526840.1:c.2210G>T	XP_011525142.1:p.Arg737Ile
XM_011526841.1:c.1796G>T	XP_011525143.1:p.Arg599Ile
XM_011526842.1:c.1649G>T	XP_011525144.1:p.Arg550Ile
XM_011526843.1:c.965G>T	XP_011525145.1:p.Arg322Ile
XM_011526844.1:c.965G>T	XP_011525146.1:p.Arg322Ile
XM_011526840.2:c.2210G>T	XP_011525142.1:p.Arg737Ile
XM_011526841.2:c.1796G>T	XP_011525143.1:p.Arg599Ile
XM_011526844.2:c.965G>T	XP_011525146.1:p.Arg322Ile
XM_017026665.1:c.3218G>T	XP_016882154.1:p.Arg1073Ile
NM_001083961.2:c.3218G>T MANE Select	NP_001077430.1:p.Arg1073Ile
NM_173636.5:c.3218G>T	NP_775907.4:p.Arg1073Ile