Canonical Allele Identifier: CA507318499

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595448T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104546T>G , CM000681.2:g.36104546T>G	GRCh38
NC_000019.9:g.36595448T>G , CM000681.1:g.36595448T>G	GRCh37
NC_000019.8:g.41287288T>G	NCBI36
NG_028101.1:g.54666T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4167T>G	ENSP00000270301.6:p.Pro1389=
ENST00000401500.7:c.4182T>G MANE Select	ENSP00000384792.1:p.Pro1394=
ENST00000587391.6:c.*4042T>G	ENSP00000465525.1:n.*4042T>G
ENST00000679357.1:c.2262T>G
ENST00000679598.1:c.927T>G
ENST00000679682.1:c.4167T>G	ENSP00000506226.1:p.Pro1389=
ENST00000679714.1:c.4176T>G	ENSP00000506627.1:p.Pro1392=
ENST00000679757.1:c.3831T>G	ENSP00000505158.1:p.Pro1277=
ENST00000679858.1:c.*3564T>G	ENSP00000505655.1:n.*3564T>G
ENST00000680211.1:c.783T>G	ENSP00000506102.1:p.Pro261=
ENST00000680280.1:n.1685T>G
ENST00000680349.1:n.2831T>G
ENST00000680403.1:c.4167T>G	ENSP00000505677.1:p.Pro1389=
ENST00000680564.1:c.3933T>G	ENSP00000505582.1:p.Pro1311=
ENST00000680590.1:c.*2562T>G	ENSP00000505350.1:n.*2562T>G
ENST00000680597.1:c.915T>G
ENST00000680739.1:c.1197T>G
ENST00000680773.1:n.2683T>G
ENST00000680806.1:c.*3485T>G	ENSP00000506418.1:n.*3485T>G
ENST00000680997.1:n.2114T>G
ENST00000681608.1:n.2027T>G
ENST00000681625.1:c.*1514T>G	ENSP00000505555.1:n.*1514T>G
ENST00000681648.1:n.2233T>G
ENST00000270301.11:c.4167T>G	ENSP00000270301.6:p.Pro1389=
ENST00000401500.6:c.4182T>G	ENSP00000384792.1:p.Pro1394=
ENST00000587391.5:c.*4042T>G	ENSP00000465525.1:n.*4042T>G
NM_001083961.1:c.4182T>G	NP_001077430.1:p.Pro1394=
NM_173636.4:c.4167T>G	NP_775907.4:p.Pro1389=
XM_005258809.2:c.4071T>G	XP_005258866.1:p.Pro1357=
XM_011526837.1:c.4167T>G	XP_011525139.1:p.Pro1389=
XM_011526838.1:c.3933T>G	XP_011525140.1:p.Pro1311=
XM_011526839.1:c.3831T>G	XP_011525141.1:p.Pro1277=
XM_011526840.1:c.3174T>G	XP_011525142.1:p.Pro1058=
XM_011526841.1:c.2760T>G	XP_011525143.1:p.Pro920=
XM_011526842.1:c.2613T>G	XP_011525144.1:p.Pro871=
XM_011526843.1:c.1929T>G	XP_011525145.1:p.Pro643=
XM_011526844.1:c.1929T>G	XP_011525146.1:p.Pro643=
XM_011526840.2:c.3174T>G	XP_011525142.1:p.Pro1058=
XM_011526841.2:c.2760T>G	XP_011525143.1:p.Pro920=
XM_011526844.2:c.1929T>G	XP_011525146.1:p.Pro643=
XM_017026665.1:c.4182T>G	XP_016882154.1:p.Pro1394=
NM_001083961.2:c.4182T>G MANE Select	NP_001077430.1:p.Pro1394=
NM_173636.5:c.4167T>G	NP_775907.4:p.Pro1389=