Canonical Allele Identifier: CA507107146

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592636C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101734C>T , CM000681.2:g.36101734C>T	GRCh38
NC_000019.9:g.36592636C>T , CM000681.1:g.36592636C>T	GRCh37
NC_000019.8:g.41284476C>T	NCBI36
NG_028101.1:g.51854C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3042C>T	ENSP00000270301.6:p.Asp1014=
ENST00000401500.7:c.3042C>T MANE Select	ENSP00000384792.1:p.Asp1014=
ENST00000587391.6:c.*2078C>T	ENSP00000465525.1:n.*2078C>T
ENST00000679357.1:c.832C>T
ENST00000679422.1:c.762-280C>T
ENST00000679682.1:c.3027C>T	ENSP00000506226.1:p.Asp1009=
ENST00000679714.1:c.3036C>T	ENSP00000506627.1:p.Asp1012=
ENST00000679757.1:c.2691C>T	ENSP00000505158.1:p.Asp897=
ENST00000679858.1:c.*2185C>T	ENSP00000505655.1:n.*2185C>T
ENST00000680211.1:c.-358C>T	ENSP00000506102.1:n.-358C>T
ENST00000680349.1:n.1025C>T
ENST00000680403.1:c.3042C>T	ENSP00000505677.1:p.Asp1014=
ENST00000680564.1:c.2971+417C>T	ENSP00000505582.1:n.2971+417C>T
ENST00000680590.1:c.*1437C>T	ENSP00000505350.1:n.*1437C>T
ENST00000680773.1:n.719C>T
ENST00000680806.1:c.*1801-280C>T	ENSP00000506418.1:n.*1801-280C>T
ENST00000680997.1:n.389C>T
ENST00000681088.1:c.704C>T
ENST00000681625.1:c.*374C>T	ENSP00000505555.1:n.*374C>T
ENST00000270301.11:c.3042C>T	ENSP00000270301.6:p.Asp1014=
ENST00000401500.6:c.3042C>T	ENSP00000384792.1:p.Asp1014=
ENST00000587391.5:c.*2078C>T	ENSP00000465525.1:n.*2078C>T
NM_001083961.1:c.3042C>T	NP_001077430.1:p.Asp1014=
NM_173636.4:c.3042C>T	NP_775907.4:p.Asp1014=
XM_005258809.2:c.2972-280C>T	XP_005258866.1:n.2972-280C>T
XM_011526837.1:c.3027C>T	XP_011525139.1:p.Asp1009=
XM_011526838.1:c.2971+417C>T	XP_011525140.1:n.2971+417C>T
XM_011526839.1:c.2691C>T	XP_011525141.1:p.Asp897=
XM_011526840.1:c.2034C>T	XP_011525142.1:p.Asp678=
XM_011526841.1:c.1620C>T	XP_011525143.1:p.Asp540=
XM_011526842.1:c.1473C>T	XP_011525144.1:p.Asp491=
XM_011526843.1:c.789C>T	XP_011525145.1:p.Asp263=
XM_011526844.1:c.789C>T	XP_011525146.1:p.Asp263=
XM_011526840.2:c.2034C>T	XP_011525142.1:p.Asp678=
XM_011526841.2:c.1620C>T	XP_011525143.1:p.Asp540=
XM_011526844.2:c.789C>T	XP_011525146.1:p.Asp263=
XM_017026665.1:c.3042C>T	XP_016882154.1:p.Asp1014=
NM_001083961.2:c.3042C>T MANE Select	NP_001077430.1:p.Asp1014=
NM_173636.5:c.3042C>T	NP_775907.4:p.Asp1014=