Canonical Allele Identifier: CA405460384

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36595443A>C (hg19) ; chr19:g.36104541A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104541A>C , CM000681.2:g.36104541A>C	GRCh38
NC_000019.9:g.36595443A>C , CM000681.1:g.36595443A>C	GRCh37
NC_000019.8:g.41287283A>C	NCBI36
NG_028101.1:g.54661A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4162A>C	ENSP00000270301.6:p.Ser1388Arg
ENST00000401500.7:c.4177A>C MANE Select	ENSP00000384792.1:p.Ser1393Arg
ENST00000587391.6:c.*4037A>C	ENSP00000465525.1:n.*4037A>C
ENST00000679357.1:c.2257A>C
ENST00000679598.1:c.922A>C
ENST00000679682.1:c.4162A>C	ENSP00000506226.1:p.Ser1388Arg
ENST00000679714.1:c.4171A>C	ENSP00000506627.1:p.Ser1391Arg
ENST00000679757.1:c.3826A>C	ENSP00000505158.1:p.Ser1276Arg
ENST00000679858.1:c.*3559A>C	ENSP00000505655.1:n.*3559A>C
ENST00000680211.1:c.778A>C	ENSP00000506102.1:p.Ser260Arg
ENST00000680280.1:n.1680A>C
ENST00000680349.1:n.2826A>C
ENST00000680403.1:c.4162A>C	ENSP00000505677.1:p.Ser1388Arg
ENST00000680564.1:c.3928A>C	ENSP00000505582.1:p.Ser1310Arg
ENST00000680590.1:c.*2557A>C	ENSP00000505350.1:n.*2557A>C
ENST00000680597.1:c.910A>C
ENST00000680739.1:c.1192A>C
ENST00000680773.1:n.2678A>C
ENST00000680806.1:c.*3480A>C	ENSP00000506418.1:n.*3480A>C
ENST00000680997.1:n.2109A>C
ENST00000681608.1:n.2022A>C
ENST00000681625.1:c.*1509A>C	ENSP00000505555.1:n.*1509A>C
ENST00000681648.1:n.2228A>C
ENST00000270301.11:c.4162A>C	ENSP00000270301.6:p.Ser1388Arg
ENST00000401500.6:c.4177A>C	ENSP00000384792.1:p.Ser1393Arg
ENST00000587391.5:c.*4037A>C	ENSP00000465525.1:n.*4037A>C
NM_001083961.1:c.4177A>C	NP_001077430.1:p.Ser1393Arg
NM_173636.4:c.4162A>C	NP_775907.4:p.Ser1388Arg
XM_005258809.2:c.4066A>C	XP_005258866.1:p.Ser1356Arg
XM_011526837.1:c.4162A>C	XP_011525139.1:p.Ser1388Arg
XM_011526838.1:c.3928A>C	XP_011525140.1:p.Ser1310Arg
XM_011526839.1:c.3826A>C	XP_011525141.1:p.Ser1276Arg
XM_011526840.1:c.3169A>C	XP_011525142.1:p.Ser1057Arg
XM_011526841.1:c.2755A>C	XP_011525143.1:p.Ser919Arg
XM_011526842.1:c.2608A>C	XP_011525144.1:p.Ser870Arg
XM_011526843.1:c.1924A>C	XP_011525145.1:p.Ser642Arg
XM_011526844.1:c.1924A>C	XP_011525146.1:p.Ser642Arg
XM_011526840.2:c.3169A>C	XP_011525142.1:p.Ser1057Arg
XM_011526841.2:c.2755A>C	XP_011525143.1:p.Ser919Arg
XM_011526844.2:c.1924A>C	XP_011525146.1:p.Ser642Arg
XM_017026665.1:c.4177A>C	XP_016882154.1:p.Ser1393Arg
NM_001083961.2:c.4177A>C MANE Select	NP_001077430.1:p.Ser1393Arg
NM_173636.5:c.4162A>C	NP_775907.4:p.Ser1388Arg