Canonical Allele Identifier: CA307843079

Gene: WDR62

Linked Data

• dbSNP Id: rs992298035
• MyVariant Identifiers: chr19:g.36595485C>T (hg19) ; chr19:g.36104583C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104583C>T , CM000681.2:g.36104583C>T	GRCh38
NC_000019.9:g.36595485C>T , CM000681.1:g.36595485C>T	GRCh37
NC_000019.8:g.41287325C>T	NCBI36
NG_028101.1:g.54703C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4204C>T	ENSP00000270301.6:p.Leu1402=
ENST00000401500.7:c.4219C>T MANE Select	ENSP00000384792.1:p.Leu1407=
ENST00000587391.6:c.*4079C>T	ENSP00000465525.1:n.*4079C>T
ENST00000679357.1:c.2299C>T
ENST00000679598.1:c.964C>T
ENST00000679682.1:c.4204C>T	ENSP00000506226.1:p.Leu1402=
ENST00000679714.1:c.4213C>T	ENSP00000506627.1:p.Leu1405=
ENST00000679757.1:c.3868C>T	ENSP00000505158.1:p.Leu1290=
ENST00000679858.1:c.*3601C>T	ENSP00000505655.1:n.*3601C>T
ENST00000680211.1:c.820C>T	ENSP00000506102.1:p.Leu274=
ENST00000680280.1:n.1722C>T
ENST00000680349.1:n.2868C>T
ENST00000680403.1:c.4204C>T	ENSP00000505677.1:p.Leu1402=
ENST00000680564.1:c.3970C>T	ENSP00000505582.1:p.Leu1324=
ENST00000680590.1:c.*2599C>T	ENSP00000505350.1:n.*2599C>T
ENST00000680597.1:c.952C>T
ENST00000680739.1:c.1234C>T
ENST00000680773.1:n.2720C>T
ENST00000680806.1:c.*3522C>T	ENSP00000506418.1:n.*3522C>T
ENST00000680997.1:n.2151C>T
ENST00000681608.1:n.2064C>T
ENST00000681625.1:c.*1551C>T	ENSP00000505555.1:n.*1551C>T
ENST00000681648.1:n.2270C>T
ENST00000270301.11:c.4204C>T	ENSP00000270301.6:p.Leu1402=
ENST00000401500.6:c.4219C>T	ENSP00000384792.1:p.Leu1407=
ENST00000587391.5:c.*4079C>T	ENSP00000465525.1:n.*4079C>T
NM_001083961.1:c.4219C>T	NP_001077430.1:p.Leu1407=
NM_173636.4:c.4204C>T	NP_775907.4:p.Leu1402=
XM_005258809.2:c.4108C>T	XP_005258866.1:p.Leu1370=
XM_011526837.1:c.4204C>T	XP_011525139.1:p.Leu1402=
XM_011526838.1:c.3970C>T	XP_011525140.1:p.Leu1324=
XM_011526839.1:c.3868C>T	XP_011525141.1:p.Leu1290=
XM_011526840.1:c.3211C>T	XP_011525142.1:p.Leu1071=
XM_011526841.1:c.2797C>T	XP_011525143.1:p.Leu933=
XM_011526842.1:c.2650C>T	XP_011525144.1:p.Leu884=
XM_011526843.1:c.1966C>T	XP_011525145.1:p.Leu656=
XM_011526844.1:c.1966C>T	XP_011525146.1:p.Leu656=
XM_011526840.2:c.3211C>T	XP_011525142.1:p.Leu1071=
XM_011526841.2:c.2797C>T	XP_011525143.1:p.Leu933=
XM_011526844.2:c.1966C>T	XP_011525146.1:p.Leu656=
XM_017026665.1:c.4219C>T	XP_016882154.1:p.Leu1407=
NM_001083961.2:c.4219C>T MANE Select	NP_001077430.1:p.Leu1407=
NM_173636.5:c.4204C>T	NP_775907.4:p.Leu1402=