Canonical Allele Identifier: CA405451841

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593692T>C (hg19) ; chr19:g.36102790T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102790T>C , CM000681.2:g.36102790T>C	GRCh38
NC_000019.9:g.36593692T>C , CM000681.1:g.36593692T>C	GRCh37
NC_000019.8:g.41285532T>C	NCBI36
NG_028101.1:g.52910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3259T>C	ENSP00000270301.6:p.Phe1087Leu
ENST00000401500.7:c.3274T>C MANE Select	ENSP00000384792.1:p.Phe1092Leu
ENST00000587391.6:c.*3134T>C	ENSP00000465525.1:n.*3134T>C
ENST00000679357.1:c.1354T>C
ENST00000679598.1:c.39T>C
ENST00000679682.1:c.3259T>C	ENSP00000506226.1:p.Phe1087Leu
ENST00000679714.1:c.3268T>C	ENSP00000506627.1:p.Phe1090Leu
ENST00000679757.1:c.2923T>C	ENSP00000505158.1:p.Phe975Leu
ENST00000679858.1:c.*2656T>C	ENSP00000505655.1:n.*2656T>C
ENST00000680211.1:c.-126T>C	ENSP00000506102.1:n.-126T>C
ENST00000680280.1:n.561T>C
ENST00000680349.1:n.1842T>C
ENST00000680403.1:c.3259T>C	ENSP00000505677.1:p.Phe1087Leu
ENST00000680564.1:c.3025T>C	ENSP00000505582.1:p.Phe1009Leu
ENST00000680590.1:c.*1654T>C	ENSP00000505350.1:n.*1654T>C
ENST00000680597.1:c.39T>C
ENST00000680739.1:c.289T>C
ENST00000680773.1:n.1775T>C
ENST00000680806.1:c.*2577T>C	ENSP00000506418.1:n.*2577T>C
ENST00000680997.1:n.1206T>C
ENST00000681608.1:n.807T>C
ENST00000681625.1:c.*606T>C	ENSP00000505555.1:n.*606T>C
ENST00000681648.1:n.573T>C
ENST00000270301.11:c.3259T>C	ENSP00000270301.6:p.Phe1087Leu
ENST00000401500.6:c.3274T>C	ENSP00000384792.1:p.Phe1092Leu
ENST00000587391.5:c.*3134T>C	ENSP00000465525.1:n.*3134T>C
NM_001083961.1:c.3274T>C	NP_001077430.1:p.Phe1092Leu
NM_173636.4:c.3259T>C	NP_775907.4:p.Phe1087Leu
XM_005258809.2:c.3163T>C	XP_005258866.1:p.Phe1055Leu
XM_011526837.1:c.3259T>C	XP_011525139.1:p.Phe1087Leu
XM_011526838.1:c.3025T>C	XP_011525140.1:p.Phe1009Leu
XM_011526839.1:c.2923T>C	XP_011525141.1:p.Phe975Leu
XM_011526840.1:c.2266T>C	XP_011525142.1:p.Phe756Leu
XM_011526841.1:c.1852T>C	XP_011525143.1:p.Phe618Leu
XM_011526842.1:c.1705T>C	XP_011525144.1:p.Phe569Leu
XM_011526843.1:c.1021T>C	XP_011525145.1:p.Phe341Leu
XM_011526844.1:c.1021T>C	XP_011525146.1:p.Phe341Leu
XM_011526840.2:c.2266T>C	XP_011525142.1:p.Phe756Leu
XM_011526841.2:c.1852T>C	XP_011525143.1:p.Phe618Leu
XM_011526844.2:c.1021T>C	XP_011525146.1:p.Phe341Leu
XM_017026665.1:c.3274T>C	XP_016882154.1:p.Phe1092Leu
NM_001083961.2:c.3274T>C MANE Select	NP_001077430.1:p.Phe1092Leu
NM_173636.5:c.3259T>C	NP_775907.4:p.Phe1087Leu