Canonical Allele Identifier: CA405450952

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593052A>T (hg19) ; chr19:g.36102150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102150A>T , CM000681.2:g.36102150A>T	GRCh38
NC_000019.9:g.36593052A>T , CM000681.1:g.36593052A>T	GRCh37
NC_000019.8:g.41284892A>T	NCBI36
NG_028101.1:g.52270A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3219A>T	ENSP00000270301.6:p.Arg1073Ser
ENST00000401500.7:c.3219A>T MANE Select	ENSP00000384792.1:p.Arg1073Ser
ENST00000587391.6:c.*2494A>T	ENSP00000465525.1:n.*2494A>T
ENST00000679357.1:c.1009A>T
ENST00000679422.1:c.898A>T
ENST00000679682.1:c.3204A>T	ENSP00000506226.1:p.Arg1068Ser
ENST00000679714.1:c.3213A>T	ENSP00000506627.1:p.Arg1071Ser
ENST00000679757.1:c.2868A>T	ENSP00000505158.1:p.Arg956Ser
ENST00000679858.1:c.*2601A>T	ENSP00000505655.1:n.*2601A>T
ENST00000680211.1:c.-181A>T	ENSP00000506102.1:n.-181A>T
ENST00000680349.1:n.1202A>T
ENST00000680403.1:c.3219A>T	ENSP00000505677.1:p.Arg1073Ser
ENST00000680564.1:c.2972-587A>T	ENSP00000505582.1:n.2972-587A>T
ENST00000680590.1:c.*1614A>T	ENSP00000505350.1:n.*1614A>T
ENST00000680739.1:c.137A>T
ENST00000680773.1:n.1135A>T
ENST00000680806.1:c.*1937A>T	ENSP00000506418.1:n.*1937A>T
ENST00000680997.1:n.566A>T
ENST00000681088.1:c.881A>T
ENST00000681608.1:n.167A>T
ENST00000681625.1:c.*551A>T	ENSP00000505555.1:n.*551A>T
ENST00000270301.11:c.3219A>T	ENSP00000270301.6:p.Arg1073Ser
ENST00000401500.6:c.3219A>T	ENSP00000384792.1:p.Arg1073Ser
ENST00000587391.5:c.*2494A>T	ENSP00000465525.1:n.*2494A>T
NM_001083961.1:c.3219A>T	NP_001077430.1:p.Arg1073Ser
NM_173636.4:c.3219A>T	NP_775907.4:p.Arg1073Ser
XM_005258809.2:c.3108A>T	XP_005258866.1:p.Arg1036Ser
XM_011526837.1:c.3204A>T	XP_011525139.1:p.Arg1068Ser
XM_011526838.1:c.2972-587A>T	XP_011525140.1:n.2972-587A>T
XM_011526839.1:c.2868A>T	XP_011525141.1:p.Arg956Ser
XM_011526840.1:c.2211A>T	XP_011525142.1:p.Arg737Ser
XM_011526841.1:c.1797A>T	XP_011525143.1:p.Arg599Ser
XM_011526842.1:c.1650A>T	XP_011525144.1:p.Arg550Ser
XM_011526843.1:c.966A>T	XP_011525145.1:p.Arg322Ser
XM_011526844.1:c.966A>T	XP_011525146.1:p.Arg322Ser
XM_011526840.2:c.2211A>T	XP_011525142.1:p.Arg737Ser
XM_011526841.2:c.1797A>T	XP_011525143.1:p.Arg599Ser
XM_011526844.2:c.966A>T	XP_011525146.1:p.Arg322Ser
XM_017026665.1:c.3219A>T	XP_016882154.1:p.Arg1073Ser
NM_001083961.2:c.3219A>T MANE Select	NP_001077430.1:p.Arg1073Ser
NM_173636.5:c.3219A>T	NP_775907.4:p.Arg1073Ser