Canonical Allele Identifier: CA507107670

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593739C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102837C>T , CM000681.2:g.36102837C>T	GRCh38
NC_000019.9:g.36593739C>T , CM000681.1:g.36593739C>T	GRCh37
NC_000019.8:g.41285579C>T	NCBI36
NG_028101.1:g.52957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3306C>T	ENSP00000270301.6:p.Leu1102=
ENST00000401500.7:c.3321C>T MANE Select	ENSP00000384792.1:p.Leu1107=
ENST00000587391.6:c.*3181C>T	ENSP00000465525.1:n.*3181C>T
ENST00000679357.1:c.1401C>T
ENST00000679598.1:c.86C>T
ENST00000679682.1:c.3306C>T	ENSP00000506226.1:p.Leu1102=
ENST00000679714.1:c.3315C>T	ENSP00000506627.1:p.Leu1105=
ENST00000679757.1:c.2970C>T	ENSP00000505158.1:p.Leu990=
ENST00000679858.1:c.*2703C>T	ENSP00000505655.1:n.*2703C>T
ENST00000680211.1:c.-79C>T	ENSP00000506102.1:n.-79C>T
ENST00000680280.1:n.608C>T
ENST00000680349.1:n.1889C>T
ENST00000680403.1:c.3306C>T	ENSP00000505677.1:p.Leu1102=
ENST00000680564.1:c.3072C>T	ENSP00000505582.1:p.Leu1024=
ENST00000680590.1:c.*1701C>T	ENSP00000505350.1:n.*1701C>T
ENST00000680597.1:c.86C>T
ENST00000680739.1:c.336C>T
ENST00000680773.1:n.1822C>T
ENST00000680806.1:c.*2624C>T	ENSP00000506418.1:n.*2624C>T
ENST00000680997.1:n.1253C>T
ENST00000681608.1:n.854C>T
ENST00000681625.1:c.*653C>T	ENSP00000505555.1:n.*653C>T
ENST00000681648.1:n.620C>T
ENST00000270301.11:c.3306C>T	ENSP00000270301.6:p.Leu1102=
ENST00000401500.6:c.3321C>T	ENSP00000384792.1:p.Leu1107=
ENST00000587391.5:c.*3181C>T	ENSP00000465525.1:n.*3181C>T
NM_001083961.1:c.3321C>T	NP_001077430.1:p.Leu1107=
NM_173636.4:c.3306C>T	NP_775907.4:p.Leu1102=
XM_005258809.2:c.3210C>T	XP_005258866.1:p.Leu1070=
XM_011526837.1:c.3306C>T	XP_011525139.1:p.Leu1102=
XM_011526838.1:c.3072C>T	XP_011525140.1:p.Leu1024=
XM_011526839.1:c.2970C>T	XP_011525141.1:p.Leu990=
XM_011526840.1:c.2313C>T	XP_011525142.1:p.Leu771=
XM_011526841.1:c.1899C>T	XP_011525143.1:p.Leu633=
XM_011526842.1:c.1752C>T	XP_011525144.1:p.Leu584=
XM_011526843.1:c.1068C>T	XP_011525145.1:p.Leu356=
XM_011526844.1:c.1068C>T	XP_011525146.1:p.Leu356=
XM_011526840.2:c.2313C>T	XP_011525142.1:p.Leu771=
XM_011526841.2:c.1899C>T	XP_011525143.1:p.Leu633=
XM_011526844.2:c.1068C>T	XP_011525146.1:p.Leu356=
XM_017026665.1:c.3321C>T	XP_016882154.1:p.Leu1107=
NM_001083961.2:c.3321C>T MANE Select	NP_001077430.1:p.Leu1107=
NM_173636.5:c.3306C>T	NP_775907.4:p.Leu1102=