Canonical Allele Identifier: CA507318455

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595433G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104531G>C , CM000681.2:g.36104531G>C	GRCh38
NC_000019.9:g.36595433G>C , CM000681.1:g.36595433G>C	GRCh37
NC_000019.8:g.41287273G>C	NCBI36
NG_028101.1:g.54651G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4152G>C	ENSP00000270301.6:p.Leu1384=
ENST00000401500.7:c.4167G>C MANE Select	ENSP00000384792.1:p.Leu1389=
ENST00000587391.6:c.*4027G>C	ENSP00000465525.1:n.*4027G>C
ENST00000679357.1:c.2247G>C
ENST00000679598.1:c.919-7G>C
ENST00000679682.1:c.4152G>C	ENSP00000506226.1:p.Leu1384=
ENST00000679714.1:c.4161G>C	ENSP00000506627.1:p.Leu1387=
ENST00000679757.1:c.3816G>C	ENSP00000505158.1:p.Leu1272=
ENST00000679858.1:c.*3549G>C	ENSP00000505655.1:n.*3549G>C
ENST00000680211.1:c.768G>C	ENSP00000506102.1:p.Leu256=
ENST00000680280.1:n.1670G>C
ENST00000680349.1:n.2816G>C
ENST00000680403.1:c.4152G>C	ENSP00000505677.1:p.Leu1384=
ENST00000680564.1:c.3918G>C	ENSP00000505582.1:p.Leu1306=
ENST00000680590.1:c.*2547G>C	ENSP00000505350.1:n.*2547G>C
ENST00000680597.1:c.900G>C
ENST00000680739.1:c.1182G>C
ENST00000680773.1:n.2668G>C
ENST00000680806.1:c.*3470G>C	ENSP00000506418.1:n.*3470G>C
ENST00000680997.1:n.2099G>C
ENST00000681608.1:n.2012G>C
ENST00000681625.1:c.*1499G>C	ENSP00000505555.1:n.*1499G>C
ENST00000681648.1:n.2218G>C
ENST00000270301.11:c.4152G>C	ENSP00000270301.6:p.Leu1384=
ENST00000401500.6:c.4167G>C	ENSP00000384792.1:p.Leu1389=
ENST00000587391.5:c.*4027G>C	ENSP00000465525.1:n.*4027G>C
NM_001083961.1:c.4167G>C	NP_001077430.1:p.Leu1389=
NM_173636.4:c.4152G>C	NP_775907.4:p.Leu1384=
XM_005258809.2:c.4056G>C	XP_005258866.1:p.Leu1352=
XM_011526837.1:c.4152G>C	XP_011525139.1:p.Leu1384=
XM_011526838.1:c.3918G>C	XP_011525140.1:p.Leu1306=
XM_011526839.1:c.3816G>C	XP_011525141.1:p.Leu1272=
XM_011526840.1:c.3159G>C	XP_011525142.1:p.Leu1053=
XM_011526841.1:c.2745G>C	XP_011525143.1:p.Leu915=
XM_011526842.1:c.2598G>C	XP_011525144.1:p.Leu866=
XM_011526843.1:c.1914G>C	XP_011525145.1:p.Leu638=
XM_011526844.1:c.1914G>C	XP_011525146.1:p.Leu638=
XM_011526840.2:c.3159G>C	XP_011525142.1:p.Leu1053=
XM_011526841.2:c.2745G>C	XP_011525143.1:p.Leu915=
XM_011526844.2:c.1914G>C	XP_011525146.1:p.Leu638=
XM_017026665.1:c.4167G>C	XP_016882154.1:p.Leu1389=
NM_001083961.2:c.4167G>C MANE Select	NP_001077430.1:p.Leu1389=
NM_173636.5:c.4152G>C	NP_775907.4:p.Leu1384=