Canonical Allele Identifier: CA507107541

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592977C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102075C>T , CM000681.2:g.36102075C>T	GRCh38
NC_000019.9:g.36592977C>T , CM000681.1:g.36592977C>T	GRCh37
NC_000019.8:g.41284817C>T	NCBI36
NG_028101.1:g.52195C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3144C>T	ENSP00000270301.6:p.Ser1048=
ENST00000401500.7:c.3144C>T MANE Select	ENSP00000384792.1:p.Ser1048=
ENST00000587391.6:c.*2419C>T	ENSP00000465525.1:n.*2419C>T
ENST00000679357.1:c.934C>T
ENST00000679422.1:c.823C>T
ENST00000679682.1:c.3129C>T	ENSP00000506226.1:p.Ser1043=
ENST00000679714.1:c.3138C>T	ENSP00000506627.1:p.Ser1046=
ENST00000679757.1:c.2793C>T	ENSP00000505158.1:p.Ser931=
ENST00000679858.1:c.*2526C>T	ENSP00000505655.1:n.*2526C>T
ENST00000680211.1:c.-256C>T	ENSP00000506102.1:n.-256C>T
ENST00000680349.1:n.1127C>T
ENST00000680403.1:c.3144C>T	ENSP00000505677.1:p.Ser1048=
ENST00000680564.1:c.2972-662C>T	ENSP00000505582.1:n.2972-662C>T
ENST00000680590.1:c.*1539C>T	ENSP00000505350.1:n.*1539C>T
ENST00000680739.1:c.62C>T
ENST00000680773.1:n.1060C>T
ENST00000680806.1:c.*1862C>T	ENSP00000506418.1:n.*1862C>T
ENST00000680997.1:n.491C>T
ENST00000681088.1:c.806C>T
ENST00000681608.1:n.92C>T
ENST00000681625.1:c.*476C>T	ENSP00000505555.1:n.*476C>T
ENST00000270301.11:c.3144C>T	ENSP00000270301.6:p.Ser1048=
ENST00000401500.6:c.3144C>T	ENSP00000384792.1:p.Ser1048=
ENST00000587391.5:c.*2419C>T	ENSP00000465525.1:n.*2419C>T
NM_001083961.1:c.3144C>T	NP_001077430.1:p.Ser1048=
NM_173636.4:c.3144C>T	NP_775907.4:p.Ser1048=
XM_005258809.2:c.3033C>T	XP_005258866.1:p.Ser1011=
XM_011526837.1:c.3129C>T	XP_011525139.1:p.Ser1043=
XM_011526838.1:c.2972-662C>T	XP_011525140.1:n.2972-662C>T
XM_011526839.1:c.2793C>T	XP_011525141.1:p.Ser931=
XM_011526840.1:c.2136C>T	XP_011525142.1:p.Ser712=
XM_011526841.1:c.1722C>T	XP_011525143.1:p.Ser574=
XM_011526842.1:c.1575C>T	XP_011525144.1:p.Ser525=
XM_011526843.1:c.891C>T	XP_011525145.1:p.Ser297=
XM_011526844.1:c.891C>T	XP_011525146.1:p.Ser297=
XM_011526840.2:c.2136C>T	XP_011525142.1:p.Ser712=
XM_011526841.2:c.1722C>T	XP_011525143.1:p.Ser574=
XM_011526844.2:c.891C>T	XP_011525146.1:p.Ser297=
XM_017026665.1:c.3144C>T	XP_016882154.1:p.Ser1048=
NM_001083961.2:c.3144C>T MANE Select	NP_001077430.1:p.Ser1048=
NM_173636.5:c.3144C>T	NP_775907.4:p.Ser1048=