Canonical Allele Identifier: CA405460914

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595509A>C (hg19) ; chr19:g.36104607A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104607A>C , CM000681.2:g.36104607A>C	GRCh38
NC_000019.9:g.36595509A>C , CM000681.1:g.36595509A>C	GRCh37
NC_000019.8:g.41287349A>C	NCBI36
NG_028101.1:g.54727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4228A>C	ENSP00000270301.6:p.Ser1410Arg
ENST00000401500.7:c.4243A>C MANE Select	ENSP00000384792.1:p.Ser1415Arg
ENST00000587391.6:c.*4103A>C	ENSP00000465525.1:n.*4103A>C
ENST00000679357.1:c.2323A>C
ENST00000679598.1:c.988A>C
ENST00000679682.1:c.4228A>C	ENSP00000506226.1:p.Ser1410Arg
ENST00000679714.1:c.4237A>C	ENSP00000506627.1:p.Ser1413Arg
ENST00000679757.1:c.3892A>C	ENSP00000505158.1:p.Ser1298Arg
ENST00000679858.1:c.*3625A>C	ENSP00000505655.1:n.*3625A>C
ENST00000680211.1:c.844A>C	ENSP00000506102.1:p.Ser282Arg
ENST00000680280.1:n.1746A>C
ENST00000680349.1:n.2892A>C
ENST00000680403.1:c.4228A>C	ENSP00000505677.1:p.Ser1410Arg
ENST00000680564.1:c.3994A>C	ENSP00000505582.1:p.Ser1332Arg
ENST00000680590.1:c.*2623A>C	ENSP00000505350.1:n.*2623A>C
ENST00000680597.1:c.976A>C
ENST00000680739.1:c.1258A>C
ENST00000680773.1:n.2744A>C
ENST00000680806.1:c.*3546A>C	ENSP00000506418.1:n.*3546A>C
ENST00000680997.1:n.2175A>C
ENST00000681608.1:n.2088A>C
ENST00000681625.1:c.*1575A>C	ENSP00000505555.1:n.*1575A>C
ENST00000681648.1:n.2294A>C
ENST00000270301.11:c.4228A>C	ENSP00000270301.6:p.Ser1410Arg
ENST00000401500.6:c.4243A>C	ENSP00000384792.1:p.Ser1415Arg
ENST00000587391.5:c.*4103A>C	ENSP00000465525.1:n.*4103A>C
NM_001083961.1:c.4243A>C	NP_001077430.1:p.Ser1415Arg
NM_173636.4:c.4228A>C	NP_775907.4:p.Ser1410Arg
XM_005258809.2:c.4132A>C	XP_005258866.1:p.Ser1378Arg
XM_011526837.1:c.4228A>C	XP_011525139.1:p.Ser1410Arg
XM_011526838.1:c.3994A>C	XP_011525140.1:p.Ser1332Arg
XM_011526839.1:c.3892A>C	XP_011525141.1:p.Ser1298Arg
XM_011526840.1:c.3235A>C	XP_011525142.1:p.Ser1079Arg
XM_011526841.1:c.2821A>C	XP_011525143.1:p.Ser941Arg
XM_011526842.1:c.2674A>C	XP_011525144.1:p.Ser892Arg
XM_011526843.1:c.1990A>C	XP_011525145.1:p.Ser664Arg
XM_011526844.1:c.1990A>C	XP_011525146.1:p.Ser664Arg
XM_011526840.2:c.3235A>C	XP_011525142.1:p.Ser1079Arg
XM_011526841.2:c.2821A>C	XP_011525143.1:p.Ser941Arg
XM_011526844.2:c.1990A>C	XP_011525146.1:p.Ser664Arg
XM_017026665.1:c.4243A>C	XP_016882154.1:p.Ser1415Arg
NM_001083961.2:c.4243A>C MANE Select	NP_001077430.1:p.Ser1415Arg
NM_173636.5:c.4228A>C	NP_775907.4:p.Ser1410Arg