Canonical Allele Identifier: CA405460334

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595432T>C (hg19) ; chr19:g.36104530T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104530T>C , CM000681.2:g.36104530T>C	GRCh38
NC_000019.9:g.36595432T>C , CM000681.1:g.36595432T>C	GRCh37
NC_000019.8:g.41287272T>C	NCBI36
NG_028101.1:g.54650T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4151T>C	ENSP00000270301.6:p.Leu1384Pro
ENST00000401500.7:c.4166T>C MANE Select	ENSP00000384792.1:p.Leu1389Pro
ENST00000587391.6:c.*4026T>C	ENSP00000465525.1:n.*4026T>C
ENST00000679357.1:c.2246T>C
ENST00000679598.1:c.919-8T>C
ENST00000679682.1:c.4151T>C	ENSP00000506226.1:p.Leu1384Pro
ENST00000679714.1:c.4160T>C	ENSP00000506627.1:p.Leu1387Pro
ENST00000679757.1:c.3815T>C	ENSP00000505158.1:p.Leu1272Pro
ENST00000679858.1:c.*3548T>C	ENSP00000505655.1:n.*3548T>C
ENST00000680211.1:c.767T>C	ENSP00000506102.1:p.Leu256Pro
ENST00000680280.1:n.1669T>C
ENST00000680349.1:n.2815T>C
ENST00000680403.1:c.4151T>C	ENSP00000505677.1:p.Leu1384Pro
ENST00000680564.1:c.3917T>C	ENSP00000505582.1:p.Leu1306Pro
ENST00000680590.1:c.*2546T>C	ENSP00000505350.1:n.*2546T>C
ENST00000680597.1:c.899T>C
ENST00000680739.1:c.1181T>C
ENST00000680773.1:n.2667T>C
ENST00000680806.1:c.*3469T>C	ENSP00000506418.1:n.*3469T>C
ENST00000680997.1:n.2098T>C
ENST00000681608.1:n.2011T>C
ENST00000681625.1:c.*1498T>C	ENSP00000505555.1:n.*1498T>C
ENST00000681648.1:n.2217T>C
ENST00000270301.11:c.4151T>C	ENSP00000270301.6:p.Leu1384Pro
ENST00000401500.6:c.4166T>C	ENSP00000384792.1:p.Leu1389Pro
ENST00000587391.5:c.*4026T>C	ENSP00000465525.1:n.*4026T>C
NM_001083961.1:c.4166T>C	NP_001077430.1:p.Leu1389Pro
NM_173636.4:c.4151T>C	NP_775907.4:p.Leu1384Pro
XM_005258809.2:c.4055T>C	XP_005258866.1:p.Leu1352Pro
XM_011526837.1:c.4151T>C	XP_011525139.1:p.Leu1384Pro
XM_011526838.1:c.3917T>C	XP_011525140.1:p.Leu1306Pro
XM_011526839.1:c.3815T>C	XP_011525141.1:p.Leu1272Pro
XM_011526840.1:c.3158T>C	XP_011525142.1:p.Leu1053Pro
XM_011526841.1:c.2744T>C	XP_011525143.1:p.Leu915Pro
XM_011526842.1:c.2597T>C	XP_011525144.1:p.Leu866Pro
XM_011526843.1:c.1913T>C	XP_011525145.1:p.Leu638Pro
XM_011526844.1:c.1913T>C	XP_011525146.1:p.Leu638Pro
XM_011526840.2:c.3158T>C	XP_011525142.1:p.Leu1053Pro
XM_011526841.2:c.2744T>C	XP_011525143.1:p.Leu915Pro
XM_011526844.2:c.1913T>C	XP_011525146.1:p.Leu638Pro
XM_017026665.1:c.4166T>C	XP_016882154.1:p.Leu1389Pro
NM_001083961.2:c.4166T>C MANE Select	NP_001077430.1:p.Leu1389Pro
NM_173636.5:c.4151T>C	NP_775907.4:p.Leu1384Pro