Canonical Allele Identifier: CA507107531

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592968C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102066C>G , CM000681.2:g.36102066C>G	GRCh38
NC_000019.9:g.36592968C>G , CM000681.1:g.36592968C>G	GRCh37
NC_000019.8:g.41284808C>G	NCBI36
NG_028101.1:g.52186C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3135C>G	ENSP00000270301.6:p.Val1045=
ENST00000401500.7:c.3135C>G MANE Select	ENSP00000384792.1:p.Val1045=
ENST00000587391.6:c.*2410C>G	ENSP00000465525.1:n.*2410C>G
ENST00000679357.1:c.925C>G
ENST00000679422.1:c.814C>G
ENST00000679682.1:c.3120C>G	ENSP00000506226.1:p.Val1040=
ENST00000679714.1:c.3129C>G	ENSP00000506627.1:p.Val1043=
ENST00000679757.1:c.2784C>G	ENSP00000505158.1:p.Val928=
ENST00000679858.1:c.*2517C>G	ENSP00000505655.1:n.*2517C>G
ENST00000680211.1:c.-265C>G	ENSP00000506102.1:n.-265C>G
ENST00000680349.1:n.1118C>G
ENST00000680403.1:c.3135C>G	ENSP00000505677.1:p.Val1045=
ENST00000680564.1:c.2972-671C>G	ENSP00000505582.1:n.2972-671C>G
ENST00000680590.1:c.*1530C>G	ENSP00000505350.1:n.*1530C>G
ENST00000680739.1:c.53C>G
ENST00000680773.1:n.1051C>G
ENST00000680806.1:c.*1853C>G	ENSP00000506418.1:n.*1853C>G
ENST00000680997.1:n.482C>G
ENST00000681088.1:c.797C>G
ENST00000681608.1:n.83C>G
ENST00000681625.1:c.*467C>G	ENSP00000505555.1:n.*467C>G
ENST00000270301.11:c.3135C>G	ENSP00000270301.6:p.Val1045=
ENST00000401500.6:c.3135C>G	ENSP00000384792.1:p.Val1045=
ENST00000587391.5:c.*2410C>G	ENSP00000465525.1:n.*2410C>G
NM_001083961.1:c.3135C>G	NP_001077430.1:p.Val1045=
NM_173636.4:c.3135C>G	NP_775907.4:p.Val1045=
XM_005258809.2:c.3024C>G	XP_005258866.1:p.Val1008=
XM_011526837.1:c.3120C>G	XP_011525139.1:p.Val1040=
XM_011526838.1:c.2972-671C>G	XP_011525140.1:n.2972-671C>G
XM_011526839.1:c.2784C>G	XP_011525141.1:p.Val928=
XM_011526840.1:c.2127C>G	XP_011525142.1:p.Val709=
XM_011526841.1:c.1713C>G	XP_011525143.1:p.Val571=
XM_011526842.1:c.1566C>G	XP_011525144.1:p.Val522=
XM_011526843.1:c.882C>G	XP_011525145.1:p.Val294=
XM_011526844.1:c.882C>G	XP_011525146.1:p.Val294=
XM_011526840.2:c.2127C>G	XP_011525142.1:p.Val709=
XM_011526841.2:c.1713C>G	XP_011525143.1:p.Val571=
XM_011526844.2:c.882C>G	XP_011525146.1:p.Val294=
XM_017026665.1:c.3135C>G	XP_016882154.1:p.Val1045=
NM_001083961.2:c.3135C>G MANE Select	NP_001077430.1:p.Val1045=
NM_173636.5:c.3135C>G	NP_775907.4:p.Val1045=