Canonical Allele Identifier: CA507107591

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593034G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102132G>C , CM000681.2:g.36102132G>C	GRCh38
NC_000019.9:g.36593034G>C , CM000681.1:g.36593034G>C	GRCh37
NC_000019.8:g.41284874G>C	NCBI36
NG_028101.1:g.52252G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3201G>C	ENSP00000270301.6:p.Leu1067=
ENST00000401500.7:c.3201G>C MANE Select	ENSP00000384792.1:p.Leu1067=
ENST00000587391.6:c.*2476G>C	ENSP00000465525.1:n.*2476G>C
ENST00000679357.1:c.991G>C
ENST00000679422.1:c.880G>C
ENST00000679682.1:c.3186G>C	ENSP00000506226.1:p.Leu1062=
ENST00000679714.1:c.3195G>C	ENSP00000506627.1:p.Leu1065=
ENST00000679757.1:c.2850G>C	ENSP00000505158.1:p.Leu950=
ENST00000679858.1:c.*2583G>C	ENSP00000505655.1:n.*2583G>C
ENST00000680211.1:c.-199G>C	ENSP00000506102.1:n.-199G>C
ENST00000680349.1:n.1184G>C
ENST00000680403.1:c.3201G>C	ENSP00000505677.1:p.Leu1067=
ENST00000680564.1:c.2972-605G>C	ENSP00000505582.1:n.2972-605G>C
ENST00000680590.1:c.*1596G>C	ENSP00000505350.1:n.*1596G>C
ENST00000680739.1:c.119G>C
ENST00000680773.1:n.1117G>C
ENST00000680806.1:c.*1919G>C	ENSP00000506418.1:n.*1919G>C
ENST00000680997.1:n.548G>C
ENST00000681088.1:c.863G>C
ENST00000681608.1:n.149G>C
ENST00000681625.1:c.*533G>C	ENSP00000505555.1:n.*533G>C
ENST00000270301.11:c.3201G>C	ENSP00000270301.6:p.Leu1067=
ENST00000401500.6:c.3201G>C	ENSP00000384792.1:p.Leu1067=
ENST00000587391.5:c.*2476G>C	ENSP00000465525.1:n.*2476G>C
NM_001083961.1:c.3201G>C	NP_001077430.1:p.Leu1067=
NM_173636.4:c.3201G>C	NP_775907.4:p.Leu1067=
XM_005258809.2:c.3090G>C	XP_005258866.1:p.Leu1030=
XM_011526837.1:c.3186G>C	XP_011525139.1:p.Leu1062=
XM_011526838.1:c.2972-605G>C	XP_011525140.1:n.2972-605G>C
XM_011526839.1:c.2850G>C	XP_011525141.1:p.Leu950=
XM_011526840.1:c.2193G>C	XP_011525142.1:p.Leu731=
XM_011526841.1:c.1779G>C	XP_011525143.1:p.Leu593=
XM_011526842.1:c.1632G>C	XP_011525144.1:p.Leu544=
XM_011526843.1:c.948G>C	XP_011525145.1:p.Leu316=
XM_011526844.1:c.948G>C	XP_011525146.1:p.Leu316=
XM_011526840.2:c.2193G>C	XP_011525142.1:p.Leu731=
XM_011526841.2:c.1779G>C	XP_011525143.1:p.Leu593=
XM_011526844.2:c.948G>C	XP_011525146.1:p.Leu316=
XM_017026665.1:c.3201G>C	XP_016882154.1:p.Leu1067=
NM_001083961.2:c.3201G>C MANE Select	NP_001077430.1:p.Leu1067=
NM_173636.5:c.3201G>C	NP_775907.4:p.Leu1067=