Canonical Allele Identifier: CA405450720

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593024T>A (hg19) ; chr19:g.36102122T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102122T>A , CM000681.2:g.36102122T>A	GRCh38
NC_000019.9:g.36593024T>A , CM000681.1:g.36593024T>A	GRCh37
NC_000019.8:g.41284864T>A	NCBI36
NG_028101.1:g.52242T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3191T>A	ENSP00000270301.6:p.Phe1064Tyr
ENST00000401500.7:c.3191T>A MANE Select	ENSP00000384792.1:p.Phe1064Tyr
ENST00000587391.6:c.*2466T>A	ENSP00000465525.1:n.*2466T>A
ENST00000679357.1:c.981T>A
ENST00000679422.1:c.870T>A
ENST00000679682.1:c.3176T>A	ENSP00000506226.1:p.Phe1059Tyr
ENST00000679714.1:c.3185T>A	ENSP00000506627.1:p.Phe1062Tyr
ENST00000679757.1:c.2840T>A	ENSP00000505158.1:p.Phe947Tyr
ENST00000679858.1:c.*2573T>A	ENSP00000505655.1:n.*2573T>A
ENST00000680211.1:c.-209T>A	ENSP00000506102.1:n.-209T>A
ENST00000680349.1:n.1174T>A
ENST00000680403.1:c.3191T>A	ENSP00000505677.1:p.Phe1064Tyr
ENST00000680564.1:c.2972-615T>A	ENSP00000505582.1:n.2972-615T>A
ENST00000680590.1:c.*1586T>A	ENSP00000505350.1:n.*1586T>A
ENST00000680739.1:c.109T>A
ENST00000680773.1:n.1107T>A
ENST00000680806.1:c.*1909T>A	ENSP00000506418.1:n.*1909T>A
ENST00000680997.1:n.538T>A
ENST00000681088.1:c.853T>A
ENST00000681608.1:n.139T>A
ENST00000681625.1:c.*523T>A	ENSP00000505555.1:n.*523T>A
ENST00000270301.11:c.3191T>A	ENSP00000270301.6:p.Phe1064Tyr
ENST00000401500.6:c.3191T>A	ENSP00000384792.1:p.Phe1064Tyr
ENST00000587391.5:c.*2466T>A	ENSP00000465525.1:n.*2466T>A
NM_001083961.1:c.3191T>A	NP_001077430.1:p.Phe1064Tyr
NM_173636.4:c.3191T>A	NP_775907.4:p.Phe1064Tyr
XM_005258809.2:c.3080T>A	XP_005258866.1:p.Phe1027Tyr
XM_011526837.1:c.3176T>A	XP_011525139.1:p.Phe1059Tyr
XM_011526838.1:c.2972-615T>A	XP_011525140.1:n.2972-615T>A
XM_011526839.1:c.2840T>A	XP_011525141.1:p.Phe947Tyr
XM_011526840.1:c.2183T>A	XP_011525142.1:p.Phe728Tyr
XM_011526841.1:c.1769T>A	XP_011525143.1:p.Phe590Tyr
XM_011526842.1:c.1622T>A	XP_011525144.1:p.Phe541Tyr
XM_011526843.1:c.938T>A	XP_011525145.1:p.Phe313Tyr
XM_011526844.1:c.938T>A	XP_011525146.1:p.Phe313Tyr
XM_011526840.2:c.2183T>A	XP_011525142.1:p.Phe728Tyr
XM_011526841.2:c.1769T>A	XP_011525143.1:p.Phe590Tyr
XM_011526844.2:c.938T>A	XP_011525146.1:p.Phe313Tyr
XM_017026665.1:c.3191T>A	XP_016882154.1:p.Phe1064Tyr
NM_001083961.2:c.3191T>A MANE Select	NP_001077430.1:p.Phe1064Tyr
NM_173636.5:c.3191T>A	NP_775907.4:p.Phe1064Tyr