Canonical Allele Identifier: CA405460342

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595435T>C (hg19) ; chr19:g.36104533T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104533T>C , CM000681.2:g.36104533T>C	GRCh38
NC_000019.9:g.36595435T>C , CM000681.1:g.36595435T>C	GRCh37
NC_000019.8:g.41287275T>C	NCBI36
NG_028101.1:g.54653T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4154T>C	ENSP00000270301.6:p.Leu1385Ser
ENST00000401500.7:c.4169T>C MANE Select	ENSP00000384792.1:p.Leu1390Ser
ENST00000587391.6:c.*4029T>C	ENSP00000465525.1:n.*4029T>C
ENST00000679357.1:c.2249T>C
ENST00000679598.1:c.919-5T>C
ENST00000679682.1:c.4154T>C	ENSP00000506226.1:p.Leu1385Ser
ENST00000679714.1:c.4163T>C	ENSP00000506627.1:p.Leu1388Ser
ENST00000679757.1:c.3818T>C	ENSP00000505158.1:p.Leu1273Ser
ENST00000679858.1:c.*3551T>C	ENSP00000505655.1:n.*3551T>C
ENST00000680211.1:c.770T>C	ENSP00000506102.1:p.Leu257Ser
ENST00000680280.1:n.1672T>C
ENST00000680349.1:n.2818T>C
ENST00000680403.1:c.4154T>C	ENSP00000505677.1:p.Leu1385Ser
ENST00000680564.1:c.3920T>C	ENSP00000505582.1:p.Leu1307Ser
ENST00000680590.1:c.*2549T>C	ENSP00000505350.1:n.*2549T>C
ENST00000680597.1:c.902T>C
ENST00000680739.1:c.1184T>C
ENST00000680773.1:n.2670T>C
ENST00000680806.1:c.*3472T>C	ENSP00000506418.1:n.*3472T>C
ENST00000680997.1:n.2101T>C
ENST00000681608.1:n.2014T>C
ENST00000681625.1:c.*1501T>C	ENSP00000505555.1:n.*1501T>C
ENST00000681648.1:n.2220T>C
ENST00000270301.11:c.4154T>C	ENSP00000270301.6:p.Leu1385Ser
ENST00000401500.6:c.4169T>C	ENSP00000384792.1:p.Leu1390Ser
ENST00000587391.5:c.*4029T>C	ENSP00000465525.1:n.*4029T>C
NM_001083961.1:c.4169T>C	NP_001077430.1:p.Leu1390Ser
NM_173636.4:c.4154T>C	NP_775907.4:p.Leu1385Ser
XM_005258809.2:c.4058T>C	XP_005258866.1:p.Leu1353Ser
XM_011526837.1:c.4154T>C	XP_011525139.1:p.Leu1385Ser
XM_011526838.1:c.3920T>C	XP_011525140.1:p.Leu1307Ser
XM_011526839.1:c.3818T>C	XP_011525141.1:p.Leu1273Ser
XM_011526840.1:c.3161T>C	XP_011525142.1:p.Leu1054Ser
XM_011526841.1:c.2747T>C	XP_011525143.1:p.Leu916Ser
XM_011526842.1:c.2600T>C	XP_011525144.1:p.Leu867Ser
XM_011526843.1:c.1916T>C	XP_011525145.1:p.Leu639Ser
XM_011526844.1:c.1916T>C	XP_011525146.1:p.Leu639Ser
XM_011526840.2:c.3161T>C	XP_011525142.1:p.Leu1054Ser
XM_011526841.2:c.2747T>C	XP_011525143.1:p.Leu916Ser
XM_011526844.2:c.1916T>C	XP_011525146.1:p.Leu639Ser
XM_017026665.1:c.4169T>C	XP_016882154.1:p.Leu1390Ser
NM_001083961.2:c.4169T>C MANE Select	NP_001077430.1:p.Leu1390Ser
NM_173636.5:c.4154T>C	NP_775907.4:p.Leu1385Ser