Canonical Allele Identifier: CA507318508

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595451C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104549C>G , CM000681.2:g.36104549C>G	GRCh38
NC_000019.9:g.36595451C>G , CM000681.1:g.36595451C>G	GRCh37
NC_000019.8:g.41287291C>G	NCBI36
NG_028101.1:g.54669C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4170C>G	ENSP00000270301.6:p.Ala1390=
ENST00000401500.7:c.4185C>G MANE Select	ENSP00000384792.1:p.Ala1395=
ENST00000587391.6:c.*4045C>G	ENSP00000465525.1:n.*4045C>G
ENST00000679357.1:c.2265C>G
ENST00000679598.1:c.930C>G
ENST00000679682.1:c.4170C>G	ENSP00000506226.1:p.Ala1390=
ENST00000679714.1:c.4179C>G	ENSP00000506627.1:p.Ala1393=
ENST00000679757.1:c.3834C>G	ENSP00000505158.1:p.Ala1278=
ENST00000679858.1:c.*3567C>G	ENSP00000505655.1:n.*3567C>G
ENST00000680211.1:c.786C>G	ENSP00000506102.1:p.Ala262=
ENST00000680280.1:n.1688C>G
ENST00000680349.1:n.2834C>G
ENST00000680403.1:c.4170C>G	ENSP00000505677.1:p.Ala1390=
ENST00000680564.1:c.3936C>G	ENSP00000505582.1:p.Ala1312=
ENST00000680590.1:c.*2565C>G	ENSP00000505350.1:n.*2565C>G
ENST00000680597.1:c.918C>G
ENST00000680739.1:c.1200C>G
ENST00000680773.1:n.2686C>G
ENST00000680806.1:c.*3488C>G	ENSP00000506418.1:n.*3488C>G
ENST00000680997.1:n.2117C>G
ENST00000681608.1:n.2030C>G
ENST00000681625.1:c.*1517C>G	ENSP00000505555.1:n.*1517C>G
ENST00000681648.1:n.2236C>G
ENST00000270301.11:c.4170C>G	ENSP00000270301.6:p.Ala1390=
ENST00000401500.6:c.4185C>G	ENSP00000384792.1:p.Ala1395=
ENST00000587391.5:c.*4045C>G	ENSP00000465525.1:n.*4045C>G
NM_001083961.1:c.4185C>G	NP_001077430.1:p.Ala1395=
NM_173636.4:c.4170C>G	NP_775907.4:p.Ala1390=
XM_005258809.2:c.4074C>G	XP_005258866.1:p.Ala1358=
XM_011526837.1:c.4170C>G	XP_011525139.1:p.Ala1390=
XM_011526838.1:c.3936C>G	XP_011525140.1:p.Ala1312=
XM_011526839.1:c.3834C>G	XP_011525141.1:p.Ala1278=
XM_011526840.1:c.3177C>G	XP_011525142.1:p.Ala1059=
XM_011526841.1:c.2763C>G	XP_011525143.1:p.Ala921=
XM_011526842.1:c.2616C>G	XP_011525144.1:p.Ala872=
XM_011526843.1:c.1932C>G	XP_011525145.1:p.Ala644=
XM_011526844.1:c.1932C>G	XP_011525146.1:p.Ala644=
XM_011526840.2:c.3177C>G	XP_011525142.1:p.Ala1059=
XM_011526841.2:c.2763C>G	XP_011525143.1:p.Ala921=
XM_011526844.2:c.1932C>G	XP_011525146.1:p.Ala644=
XM_017026665.1:c.4185C>G	XP_016882154.1:p.Ala1395=
NM_001083961.2:c.4185C>G MANE Select	NP_001077430.1:p.Ala1395=
NM_173636.5:c.4170C>G	NP_775907.4:p.Ala1390=