Canonical Allele Identifier: CA405449917

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102022-G-C
• MyVariant Identifiers: chr19:g.36592924G>C (hg19) ; chr19:g.36102022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102022G>C , CM000681.2:g.36102022G>C	GRCh38
NC_000019.9:g.36592924G>C , CM000681.1:g.36592924G>C	GRCh37
NC_000019.8:g.41284764G>C	NCBI36
NG_028101.1:g.52142G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3091G>C	ENSP00000270301.6:p.Gly1031Arg
ENST00000401500.7:c.3091G>C MANE Select	ENSP00000384792.1:p.Gly1031Arg
ENST00000587391.6:c.*2366G>C	ENSP00000465525.1:n.*2366G>C
ENST00000679357.1:c.881G>C
ENST00000679422.1:c.770G>C
ENST00000679682.1:c.3076G>C	ENSP00000506226.1:p.Gly1026Arg
ENST00000679714.1:c.3085G>C	ENSP00000506627.1:p.Gly1029Arg
ENST00000679757.1:c.2740G>C	ENSP00000505158.1:p.Gly914Arg
ENST00000679858.1:c.*2473G>C	ENSP00000505655.1:n.*2473G>C
ENST00000680211.1:c.-309G>C	ENSP00000506102.1:n.-309G>C
ENST00000680349.1:n.1074G>C
ENST00000680403.1:c.3091G>C	ENSP00000505677.1:p.Gly1031Arg
ENST00000680564.1:c.2971+705G>C	ENSP00000505582.1:n.2971+705G>C
ENST00000680590.1:c.*1486G>C	ENSP00000505350.1:n.*1486G>C
ENST00000680739.1:c.9G>C
ENST00000680773.1:n.1007G>C
ENST00000680806.1:c.*1809G>C	ENSP00000506418.1:n.*1809G>C
ENST00000680997.1:n.438G>C
ENST00000681088.1:c.753G>C
ENST00000681608.1:n.39G>C
ENST00000681625.1:c.*423G>C	ENSP00000505555.1:n.*423G>C
ENST00000270301.11:c.3091G>C	ENSP00000270301.6:p.Gly1031Arg
ENST00000401500.6:c.3091G>C	ENSP00000384792.1:p.Gly1031Arg
ENST00000587391.5:c.*2366G>C	ENSP00000465525.1:n.*2366G>C
NM_001083961.1:c.3091G>C	NP_001077430.1:p.Gly1031Arg
NM_173636.4:c.3091G>C	NP_775907.4:p.Gly1031Arg
XM_005258809.2:c.2980G>C	XP_005258866.1:p.Gly994Arg
XM_011526837.1:c.3076G>C	XP_011525139.1:p.Gly1026Arg
XM_011526838.1:c.2971+705G>C	XP_011525140.1:n.2971+705G>C
XM_011526839.1:c.2740G>C	XP_011525141.1:p.Gly914Arg
XM_011526840.1:c.2083G>C	XP_011525142.1:p.Gly695Arg
XM_011526841.1:c.1669G>C	XP_011525143.1:p.Gly557Arg
XM_011526842.1:c.1522G>C	XP_011525144.1:p.Gly508Arg
XM_011526843.1:c.838G>C	XP_011525145.1:p.Gly280Arg
XM_011526844.1:c.838G>C	XP_011525146.1:p.Gly280Arg
XM_011526840.2:c.2083G>C	XP_011525142.1:p.Gly695Arg
XM_011526841.2:c.1669G>C	XP_011525143.1:p.Gly557Arg
XM_011526844.2:c.838G>C	XP_011525146.1:p.Gly280Arg
XM_017026665.1:c.3091G>C	XP_016882154.1:p.Gly1031Arg
NM_001083961.2:c.3091G>C MANE Select	NP_001077430.1:p.Gly1031Arg
NM_173636.5:c.3091G>C	NP_775907.4:p.Gly1031Arg