Canonical Allele Identifier: CA507317808

Gene: WDR62

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3343C>A	ENSP00000270301.6:p.Arg1115=
ENST00000401500.7:c.3358C>A MANE Select	ENSP00000384792.1:p.Arg1120=
ENST00000587391.6:c.*3218C>A	ENSP00000465525.1:n.*3218C>A
ENST00000679357.1:c.1438C>A
ENST00000679598.1:c.123C>A
ENST00000679682.1:c.3343C>A	ENSP00000506226.1:p.Arg1115=
ENST00000679714.1:c.3352C>A	ENSP00000506627.1:p.Arg1118=
ENST00000679757.1:c.3007C>A	ENSP00000505158.1:p.Arg1003=
ENST00000679858.1:c.*2740C>A	ENSP00000505655.1:n.*2740C>A
ENST00000680211.1:c.-42C>A	ENSP00000506102.1:n.-42C>A
ENST00000680280.1:n.645C>A
ENST00000680349.1:n.1926C>A
ENST00000680403.1:c.3343C>A	ENSP00000505677.1:p.Arg1115=
ENST00000680564.1:c.3109C>A	ENSP00000505582.1:p.Arg1037=
ENST00000680590.1:c.*1738C>A	ENSP00000505350.1:n.*1738C>A
ENST00000680597.1:c.123C>A
ENST00000680739.1:c.373C>A
ENST00000680773.1:n.1859C>A
ENST00000680806.1:c.*2661C>A	ENSP00000506418.1:n.*2661C>A
ENST00000680997.1:n.1290C>A
ENST00000681608.1:n.987C>A
ENST00000681625.1:c.*690C>A	ENSP00000505555.1:n.*690C>A
ENST00000681648.1:n.657C>A
ENST00000270301.11:c.3343C>A	ENSP00000270301.6:p.Arg1115=
ENST00000401500.6:c.3358C>A	ENSP00000384792.1:p.Arg1120=
ENST00000587391.5:c.*3218C>A	ENSP00000465525.1:n.*3218C>A
NM_001083961.1:c.3358C>A	NP_001077430.1:p.Arg1120=
NM_173636.4:c.3343C>A	NP_775907.4:p.Arg1115=
XM_005258809.2:c.3247C>A	XP_005258866.1:p.Arg1083=
XM_011526837.1:c.3343C>A	XP_011525139.1:p.Arg1115=
XM_011526838.1:c.3109C>A	XP_011525140.1:p.Arg1037=
XM_011526839.1:c.3007C>A	XP_011525141.1:p.Arg1003=
XM_011526840.1:c.2350C>A	XP_011525142.1:p.Arg784=
XM_011526841.1:c.1936C>A	XP_011525143.1:p.Arg646=
XM_011526842.1:c.1789C>A	XP_011525144.1:p.Arg597=
XM_011526843.1:c.1105C>A	XP_011525145.1:p.Arg369=
XM_011526844.1:c.1105C>A	XP_011525146.1:p.Arg369=
XM_011526840.2:c.2350C>A	XP_011525142.1:p.Arg784=
XM_011526841.2:c.1936C>A	XP_011525143.1:p.Arg646=
XM_011526844.2:c.1105C>A	XP_011525146.1:p.Arg369=
XM_017026665.1:c.3358C>A	XP_016882154.1:p.Arg1120=
NM_001083961.2:c.3358C>A MANE Select	NP_001077430.1:p.Arg1120=
NM_173636.5:c.3343C>A	NP_775907.4:p.Arg1115=