Canonical Allele Identifier: CA405460462

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595458A>G (hg19) ; chr19:g.36104556A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104556A>G , CM000681.2:g.36104556A>G	GRCh38
NC_000019.9:g.36595458A>G , CM000681.1:g.36595458A>G	GRCh37
NC_000019.8:g.41287298A>G	NCBI36
NG_028101.1:g.54676A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4177A>G	ENSP00000270301.6:p.Ser1393Gly
ENST00000401500.7:c.4192A>G MANE Select	ENSP00000384792.1:p.Ser1398Gly
ENST00000587391.6:c.*4052A>G	ENSP00000465525.1:n.*4052A>G
ENST00000679357.1:c.2272A>G
ENST00000679598.1:c.937A>G
ENST00000679682.1:c.4177A>G	ENSP00000506226.1:p.Ser1393Gly
ENST00000679714.1:c.4186A>G	ENSP00000506627.1:p.Ser1396Gly
ENST00000679757.1:c.3841A>G	ENSP00000505158.1:p.Ser1281Gly
ENST00000679858.1:c.*3574A>G	ENSP00000505655.1:n.*3574A>G
ENST00000680211.1:c.793A>G	ENSP00000506102.1:p.Ser265Gly
ENST00000680280.1:n.1695A>G
ENST00000680349.1:n.2841A>G
ENST00000680403.1:c.4177A>G	ENSP00000505677.1:p.Ser1393Gly
ENST00000680564.1:c.3943A>G	ENSP00000505582.1:p.Ser1315Gly
ENST00000680590.1:c.*2572A>G	ENSP00000505350.1:n.*2572A>G
ENST00000680597.1:c.925A>G
ENST00000680739.1:c.1207A>G
ENST00000680773.1:n.2693A>G
ENST00000680806.1:c.*3495A>G	ENSP00000506418.1:n.*3495A>G
ENST00000680997.1:n.2124A>G
ENST00000681608.1:n.2037A>G
ENST00000681625.1:c.*1524A>G	ENSP00000505555.1:n.*1524A>G
ENST00000681648.1:n.2243A>G
ENST00000270301.11:c.4177A>G	ENSP00000270301.6:p.Ser1393Gly
ENST00000401500.6:c.4192A>G	ENSP00000384792.1:p.Ser1398Gly
ENST00000587391.5:c.*4052A>G	ENSP00000465525.1:n.*4052A>G
NM_001083961.1:c.4192A>G	NP_001077430.1:p.Ser1398Gly
NM_173636.4:c.4177A>G	NP_775907.4:p.Ser1393Gly
XM_005258809.2:c.4081A>G	XP_005258866.1:p.Ser1361Gly
XM_011526837.1:c.4177A>G	XP_011525139.1:p.Ser1393Gly
XM_011526838.1:c.3943A>G	XP_011525140.1:p.Ser1315Gly
XM_011526839.1:c.3841A>G	XP_011525141.1:p.Ser1281Gly
XM_011526840.1:c.3184A>G	XP_011525142.1:p.Ser1062Gly
XM_011526841.1:c.2770A>G	XP_011525143.1:p.Ser924Gly
XM_011526842.1:c.2623A>G	XP_011525144.1:p.Ser875Gly
XM_011526843.1:c.1939A>G	XP_011525145.1:p.Ser647Gly
XM_011526844.1:c.1939A>G	XP_011525146.1:p.Ser647Gly
XM_011526840.2:c.3184A>G	XP_011525142.1:p.Ser1062Gly
XM_011526841.2:c.2770A>G	XP_011525143.1:p.Ser924Gly
XM_011526844.2:c.1939A>G	XP_011525146.1:p.Ser647Gly
XM_017026665.1:c.4192A>G	XP_016882154.1:p.Ser1398Gly
NM_001083961.2:c.4192A>G MANE Select	NP_001077430.1:p.Ser1398Gly
NM_173636.5:c.4177A>G	NP_775907.4:p.Ser1393Gly