Canonical Allele Identifier: CA405452737

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102970-C-G
• MyVariant Identifiers: chr19:g.36593872C>G (hg19) ; chr19:g.36102970C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102970C>G , CM000681.2:g.36102970C>G	GRCh38
NC_000019.9:g.36593872C>G , CM000681.1:g.36593872C>G	GRCh37
NC_000019.8:g.41285712C>G	NCBI36
NG_028101.1:g.53090C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3343C>G	ENSP00000270301.6:p.Arg1115Gly
ENST00000401500.7:c.3358C>G MANE Select	ENSP00000384792.1:p.Arg1120Gly
ENST00000587391.6:c.*3218C>G	ENSP00000465525.1:n.*3218C>G
ENST00000679357.1:c.1438C>G
ENST00000679598.1:c.123C>G
ENST00000679682.1:c.3343C>G	ENSP00000506226.1:p.Arg1115Gly
ENST00000679714.1:c.3352C>G	ENSP00000506627.1:p.Arg1118Gly
ENST00000679757.1:c.3007C>G	ENSP00000505158.1:p.Arg1003Gly
ENST00000679858.1:c.*2740C>G	ENSP00000505655.1:n.*2740C>G
ENST00000680211.1:c.-42C>G	ENSP00000506102.1:n.-42C>G
ENST00000680280.1:n.645C>G
ENST00000680349.1:n.1926C>G
ENST00000680403.1:c.3343C>G	ENSP00000505677.1:p.Arg1115Gly
ENST00000680564.1:c.3109C>G	ENSP00000505582.1:p.Arg1037Gly
ENST00000680590.1:c.*1738C>G	ENSP00000505350.1:n.*1738C>G
ENST00000680597.1:c.123C>G
ENST00000680739.1:c.373C>G
ENST00000680773.1:n.1859C>G
ENST00000680806.1:c.*2661C>G	ENSP00000506418.1:n.*2661C>G
ENST00000680997.1:n.1290C>G
ENST00000681608.1:n.987C>G
ENST00000681625.1:c.*690C>G	ENSP00000505555.1:n.*690C>G
ENST00000681648.1:n.657C>G
ENST00000270301.11:c.3343C>G	ENSP00000270301.6:p.Arg1115Gly
ENST00000401500.6:c.3358C>G	ENSP00000384792.1:p.Arg1120Gly
ENST00000587391.5:c.*3218C>G	ENSP00000465525.1:n.*3218C>G
NM_001083961.1:c.3358C>G	NP_001077430.1:p.Arg1120Gly
NM_173636.4:c.3343C>G	NP_775907.4:p.Arg1115Gly
XM_005258809.2:c.3247C>G	XP_005258866.1:p.Arg1083Gly
XM_011526837.1:c.3343C>G	XP_011525139.1:p.Arg1115Gly
XM_011526838.1:c.3109C>G	XP_011525140.1:p.Arg1037Gly
XM_011526839.1:c.3007C>G	XP_011525141.1:p.Arg1003Gly
XM_011526840.1:c.2350C>G	XP_011525142.1:p.Arg784Gly
XM_011526841.1:c.1936C>G	XP_011525143.1:p.Arg646Gly
XM_011526842.1:c.1789C>G	XP_011525144.1:p.Arg597Gly
XM_011526843.1:c.1105C>G	XP_011525145.1:p.Arg369Gly
XM_011526844.1:c.1105C>G	XP_011525146.1:p.Arg369Gly
XM_011526840.2:c.2350C>G	XP_011525142.1:p.Arg784Gly
XM_011526841.2:c.1936C>G	XP_011525143.1:p.Arg646Gly
XM_011526844.2:c.1105C>G	XP_011525146.1:p.Arg369Gly
XM_017026665.1:c.3358C>G	XP_016882154.1:p.Arg1120Gly
NM_001083961.2:c.3358C>G MANE Select	NP_001077430.1:p.Arg1120Gly
NM_173636.5:c.3343C>G	NP_775907.4:p.Arg1115Gly