Canonical Allele Identifier: CA405461090

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595529G>C (hg19) ; chr19:g.36104627G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104627G>C , CM000681.2:g.36104627G>C	GRCh38
NC_000019.9:g.36595529G>C , CM000681.1:g.36595529G>C	GRCh37
NC_000019.8:g.41287369G>C	NCBI36
NG_028101.1:g.54747G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4248G>C	ENSP00000270301.6:p.Leu1416Phe
ENST00000401500.7:c.4263G>C MANE Select	ENSP00000384792.1:p.Leu1421Phe
ENST00000587391.6:c.*4123G>C	ENSP00000465525.1:n.*4123G>C
ENST00000679357.1:c.2343G>C
ENST00000679598.1:c.1008G>C
ENST00000679682.1:c.4248G>C	ENSP00000506226.1:p.Leu1416Phe
ENST00000679714.1:c.4257G>C	ENSP00000506627.1:p.Leu1419Phe
ENST00000679757.1:c.3912G>C	ENSP00000505158.1:p.Leu1304Phe
ENST00000679858.1:c.*3645G>C	ENSP00000505655.1:n.*3645G>C
ENST00000680211.1:c.864G>C	ENSP00000506102.1:p.Leu288Phe
ENST00000680280.1:n.1766G>C
ENST00000680349.1:n.2912G>C
ENST00000680403.1:c.4248G>C	ENSP00000505677.1:p.Leu1416Phe
ENST00000680564.1:c.4014G>C	ENSP00000505582.1:p.Leu1338Phe
ENST00000680590.1:c.*2643G>C	ENSP00000505350.1:n.*2643G>C
ENST00000680597.1:c.996G>C
ENST00000680739.1:c.1278G>C
ENST00000680773.1:n.2764G>C
ENST00000680806.1:c.*3566G>C	ENSP00000506418.1:n.*3566G>C
ENST00000680997.1:n.2195G>C
ENST00000681608.1:n.2108G>C
ENST00000681625.1:c.*1595G>C	ENSP00000505555.1:n.*1595G>C
ENST00000681648.1:n.2314G>C
ENST00000270301.11:c.4248G>C	ENSP00000270301.6:p.Leu1416Phe
ENST00000401500.6:c.4263G>C	ENSP00000384792.1:p.Leu1421Phe
ENST00000587391.5:c.*4123G>C	ENSP00000465525.1:n.*4123G>C
NM_001083961.1:c.4263G>C	NP_001077430.1:p.Leu1421Phe
NM_173636.4:c.4248G>C	NP_775907.4:p.Leu1416Phe
XM_005258809.2:c.4152G>C	XP_005258866.1:p.Leu1384Phe
XM_011526837.1:c.4248G>C	XP_011525139.1:p.Leu1416Phe
XM_011526838.1:c.4014G>C	XP_011525140.1:p.Leu1338Phe
XM_011526839.1:c.3912G>C	XP_011525141.1:p.Leu1304Phe
XM_011526840.1:c.3255G>C	XP_011525142.1:p.Leu1085Phe
XM_011526841.1:c.2841G>C	XP_011525143.1:p.Leu947Phe
XM_011526842.1:c.2694G>C	XP_011525144.1:p.Leu898Phe
XM_011526843.1:c.2010G>C	XP_011525145.1:p.Leu670Phe
XM_011526844.1:c.2010G>C	XP_011525146.1:p.Leu670Phe
XM_011526840.2:c.3255G>C	XP_011525142.1:p.Leu1085Phe
XM_011526841.2:c.2841G>C	XP_011525143.1:p.Leu947Phe
XM_011526844.2:c.2010G>C	XP_011525146.1:p.Leu670Phe
XM_017026665.1:c.4263G>C	XP_016882154.1:p.Leu1421Phe
NM_001083961.2:c.4263G>C MANE Select	NP_001077430.1:p.Leu1421Phe
NM_173636.5:c.4248G>C	NP_775907.4:p.Leu1416Phe