Canonical Allele Identifier: CA507318707

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595520G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104618G>C , CM000681.2:g.36104618G>C	GRCh38
NC_000019.9:g.36595520G>C , CM000681.1:g.36595520G>C	GRCh37
NC_000019.8:g.41287360G>C	NCBI36
NG_028101.1:g.54738G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.4239G>C	ENSP00000270301.6:p.Gly1413=
ENST00000401500.7:c.4254G>C MANE Select	ENSP00000384792.1:p.Gly1418=
ENST00000587391.6:c.*4114G>C	ENSP00000465525.1:n.*4114G>C
ENST00000679357.1:c.2334G>C
ENST00000679598.1:c.999G>C
ENST00000679682.1:c.4239G>C	ENSP00000506226.1:p.Gly1413=
ENST00000679714.1:c.4248G>C	ENSP00000506627.1:p.Gly1416=
ENST00000679757.1:c.3903G>C	ENSP00000505158.1:p.Gly1301=
ENST00000679858.1:c.*3636G>C	ENSP00000505655.1:n.*3636G>C
ENST00000680211.1:c.855G>C	ENSP00000506102.1:p.Gly285=
ENST00000680280.1:n.1757G>C
ENST00000680349.1:n.2903G>C
ENST00000680403.1:c.4239G>C	ENSP00000505677.1:p.Gly1413=
ENST00000680564.1:c.4005G>C	ENSP00000505582.1:p.Gly1335=
ENST00000680590.1:c.*2634G>C	ENSP00000505350.1:n.*2634G>C
ENST00000680597.1:c.987G>C
ENST00000680739.1:c.1269G>C
ENST00000680773.1:n.2755G>C
ENST00000680806.1:c.*3557G>C	ENSP00000506418.1:n.*3557G>C
ENST00000680997.1:n.2186G>C
ENST00000681608.1:n.2099G>C
ENST00000681625.1:c.*1586G>C	ENSP00000505555.1:n.*1586G>C
ENST00000681648.1:n.2305G>C
ENST00000270301.11:c.4239G>C	ENSP00000270301.6:p.Gly1413=
ENST00000401500.6:c.4254G>C	ENSP00000384792.1:p.Gly1418=
ENST00000587391.5:c.*4114G>C	ENSP00000465525.1:n.*4114G>C
NM_001083961.1:c.4254G>C	NP_001077430.1:p.Gly1418=
NM_173636.4:c.4239G>C	NP_775907.4:p.Gly1413=
XM_005258809.2:c.4143G>C	XP_005258866.1:p.Gly1381=
XM_011526837.1:c.4239G>C	XP_011525139.1:p.Gly1413=
XM_011526838.1:c.4005G>C	XP_011525140.1:p.Gly1335=
XM_011526839.1:c.3903G>C	XP_011525141.1:p.Gly1301=
XM_011526840.1:c.3246G>C	XP_011525142.1:p.Gly1082=
XM_011526841.1:c.2832G>C	XP_011525143.1:p.Gly944=
XM_011526842.1:c.2685G>C	XP_011525144.1:p.Gly895=
XM_011526843.1:c.2001G>C	XP_011525145.1:p.Gly667=
XM_011526844.1:c.2001G>C	XP_011525146.1:p.Gly667=
XM_011526840.2:c.3246G>C	XP_011525142.1:p.Gly1082=
XM_011526841.2:c.2832G>C	XP_011525143.1:p.Gly944=
XM_011526844.2:c.2001G>C	XP_011525146.1:p.Gly667=
XM_017026665.1:c.4254G>C	XP_016882154.1:p.Gly1418=
NM_001083961.2:c.4254G>C MANE Select	NP_001077430.1:p.Gly1418=
NM_173636.5:c.4239G>C	NP_775907.4:p.Gly1413=