Canonical Allele Identifier: CA405449863

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592916G>T (hg19) ; chr19:g.36102014G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102014G>T , CM000681.2:g.36102014G>T	GRCh38
NC_000019.9:g.36592916G>T , CM000681.1:g.36592916G>T	GRCh37
NC_000019.8:g.41284756G>T	NCBI36
NG_028101.1:g.52134G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3083G>T	ENSP00000270301.6:p.Gly1028Val
ENST00000401500.7:c.3083G>T MANE Select	ENSP00000384792.1:p.Gly1028Val
ENST00000587391.6:c.*2358G>T	ENSP00000465525.1:n.*2358G>T
ENST00000679357.1:c.873G>T
ENST00000679422.1:c.762G>T
ENST00000679682.1:c.3068G>T	ENSP00000506226.1:p.Gly1023Val
ENST00000679714.1:c.3077G>T	ENSP00000506627.1:p.Gly1026Val
ENST00000679757.1:c.2732G>T	ENSP00000505158.1:p.Gly911Val
ENST00000679858.1:c.*2465G>T	ENSP00000505655.1:n.*2465G>T
ENST00000680211.1:c.-317G>T	ENSP00000506102.1:n.-317G>T
ENST00000680349.1:n.1066G>T
ENST00000680403.1:c.3083G>T	ENSP00000505677.1:p.Gly1028Val
ENST00000680564.1:c.2971+697G>T	ENSP00000505582.1:n.2971+697G>T
ENST00000680590.1:c.*1478G>T	ENSP00000505350.1:n.*1478G>T
ENST00000680739.1:c.1G>T
ENST00000680773.1:n.999G>T
ENST00000680806.1:c.*1801G>T	ENSP00000506418.1:n.*1801G>T
ENST00000680997.1:n.430G>T
ENST00000681088.1:c.745G>T
ENST00000681608.1:n.31G>T
ENST00000681625.1:c.*415G>T	ENSP00000505555.1:n.*415G>T
ENST00000270301.11:c.3083G>T	ENSP00000270301.6:p.Gly1028Val
ENST00000401500.6:c.3083G>T	ENSP00000384792.1:p.Gly1028Val
ENST00000587391.5:c.*2358G>T	ENSP00000465525.1:n.*2358G>T
NM_001083961.1:c.3083G>T	NP_001077430.1:p.Gly1028Val
NM_173636.4:c.3083G>T	NP_775907.4:p.Gly1028Val
XM_005258809.2:c.2972G>T	XP_005258866.1:p.Gly991Val
XM_011526837.1:c.3068G>T	XP_011525139.1:p.Gly1023Val
XM_011526838.1:c.2971+697G>T	XP_011525140.1:n.2971+697G>T
XM_011526839.1:c.2732G>T	XP_011525141.1:p.Gly911Val
XM_011526840.1:c.2075G>T	XP_011525142.1:p.Gly692Val
XM_011526841.1:c.1661G>T	XP_011525143.1:p.Gly554Val
XM_011526842.1:c.1514G>T	XP_011525144.1:p.Gly505Val
XM_011526843.1:c.830G>T	XP_011525145.1:p.Gly277Val
XM_011526844.1:c.830G>T	XP_011525146.1:p.Gly277Val
XM_011526840.2:c.2075G>T	XP_011525142.1:p.Gly692Val
XM_011526841.2:c.1661G>T	XP_011525143.1:p.Gly554Val
XM_011526844.2:c.830G>T	XP_011525146.1:p.Gly277Val
XM_017026665.1:c.3083G>T	XP_016882154.1:p.Gly1028Val
NM_001083961.2:c.3083G>T MANE Select	NP_001077430.1:p.Gly1028Val
NM_173636.5:c.3083G>T	NP_775907.4:p.Gly1028Val