Canonical Allele Identifier: CA405457538

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36594455T>C (hg19) ; chr19:g.36103553T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36103553T>C , CM000681.2:g.36103553T>C	GRCh38
NC_000019.9:g.36594455T>C , CM000681.1:g.36594455T>C	GRCh37
NC_000019.8:g.41286295T>C	NCBI36
NG_028101.1:g.53673T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3710T>C	ENSP00000270301.6:p.Val1237Ala
ENST00000401500.7:c.3725T>C MANE Select	ENSP00000384792.1:p.Val1242Ala
ENST00000587391.6:c.*3585T>C	ENSP00000465525.1:n.*3585T>C
ENST00000679357.1:c.1805T>C
ENST00000679598.1:c.490T>C
ENST00000679682.1:c.3710T>C	ENSP00000506226.1:p.Val1237Ala
ENST00000679714.1:c.3719T>C	ENSP00000506627.1:p.Val1240Ala
ENST00000679757.1:c.3374T>C	ENSP00000505158.1:p.Val1125Ala
ENST00000679858.1:c.*3107T>C	ENSP00000505655.1:n.*3107T>C
ENST00000680211.1:c.326T>C	ENSP00000506102.1:p.Val109Ala
ENST00000680280.1:n.1228T>C
ENST00000680349.1:n.2374T>C
ENST00000680403.1:c.3710T>C	ENSP00000505677.1:p.Val1237Ala
ENST00000680564.1:c.3476T>C	ENSP00000505582.1:p.Val1159Ala
ENST00000680590.1:c.*2105T>C	ENSP00000505350.1:n.*2105T>C
ENST00000680597.1:c.458T>C
ENST00000680739.1:c.740T>C
ENST00000680773.1:n.2226T>C
ENST00000680806.1:c.*3028T>C	ENSP00000506418.1:n.*3028T>C
ENST00000680997.1:n.1657T>C
ENST00000681608.1:n.1570T>C
ENST00000681625.1:c.*1057T>C	ENSP00000505555.1:n.*1057T>C
ENST00000681648.1:n.1240T>C
ENST00000270301.11:c.3710T>C	ENSP00000270301.6:p.Val1237Ala
ENST00000401500.6:c.3725T>C	ENSP00000384792.1:p.Val1242Ala
ENST00000587391.5:c.*3585T>C	ENSP00000465525.1:n.*3585T>C
NM_001083961.1:c.3725T>C	NP_001077430.1:p.Val1242Ala
NM_173636.4:c.3710T>C	NP_775907.4:p.Val1237Ala
XM_005258809.2:c.3614T>C	XP_005258866.1:p.Val1205Ala
XM_011526837.1:c.3710T>C	XP_011525139.1:p.Val1237Ala
XM_011526838.1:c.3476T>C	XP_011525140.1:p.Val1159Ala
XM_011526839.1:c.3374T>C	XP_011525141.1:p.Val1125Ala
XM_011526840.1:c.2717T>C	XP_011525142.1:p.Val906Ala
XM_011526841.1:c.2303T>C	XP_011525143.1:p.Val768Ala
XM_011526842.1:c.2156T>C	XP_011525144.1:p.Val719Ala
XM_011526843.1:c.1472T>C	XP_011525145.1:p.Val491Ala
XM_011526844.1:c.1472T>C	XP_011525146.1:p.Val491Ala
XM_011526840.2:c.2717T>C	XP_011525142.1:p.Val906Ala
XM_011526841.2:c.2303T>C	XP_011525143.1:p.Val768Ala
XM_011526844.2:c.1472T>C	XP_011525146.1:p.Val491Ala
XM_017026665.1:c.3725T>C	XP_016882154.1:p.Val1242Ala
NM_001083961.2:c.3725T>C MANE Select	NP_001077430.1:p.Val1242Ala
NM_173636.5:c.3710T>C	NP_775907.4:p.Val1237Ala