Canonical Allele Identifier: CA405449165

Gene: WDR62

Linked Data

• dbSNP Id: rs1973349660
• MyVariant Identifiers: chr19:g.36592601T>C (hg19) ; chr19:g.36101699T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101699T>C , CM000681.2:g.36101699T>C	GRCh38
NC_000019.9:g.36592601T>C , CM000681.1:g.36592601T>C	GRCh37
NC_000019.8:g.41284441T>C	NCBI36
NG_028101.1:g.51819T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3007T>C	ENSP00000270301.6:p.Phe1003Leu
ENST00000401500.7:c.3007T>C MANE Select	ENSP00000384792.1:p.Phe1003Leu
ENST00000587391.6:c.*2043T>C	ENSP00000465525.1:n.*2043T>C
ENST00000679357.1:c.797T>C
ENST00000679422.1:c.762-315T>C
ENST00000679682.1:c.2992T>C	ENSP00000506226.1:p.Phe998Leu
ENST00000679714.1:c.3001T>C	ENSP00000506627.1:p.Phe1001Leu
ENST00000679757.1:c.2656T>C	ENSP00000505158.1:p.Phe886Leu
ENST00000679858.1:c.*2150T>C	ENSP00000505655.1:n.*2150T>C
ENST00000680211.1:c.-393T>C	ENSP00000506102.1:n.-393T>C
ENST00000680349.1:n.990T>C
ENST00000680403.1:c.3007T>C	ENSP00000505677.1:p.Phe1003Leu
ENST00000680564.1:c.2971+382T>C	ENSP00000505582.1:n.2971+382T>C
ENST00000680590.1:c.*1402T>C	ENSP00000505350.1:n.*1402T>C
ENST00000680773.1:n.684T>C
ENST00000680806.1:c.*1801-315T>C	ENSP00000506418.1:n.*1801-315T>C
ENST00000680997.1:n.354T>C
ENST00000681088.1:c.669T>C
ENST00000681625.1:c.*339T>C	ENSP00000505555.1:n.*339T>C
ENST00000270301.11:c.3007T>C	ENSP00000270301.6:p.Phe1003Leu
ENST00000401500.6:c.3007T>C	ENSP00000384792.1:p.Phe1003Leu
ENST00000587391.5:c.*2043T>C	ENSP00000465525.1:n.*2043T>C
NM_001083961.1:c.3007T>C	NP_001077430.1:p.Phe1003Leu
NM_173636.4:c.3007T>C	NP_775907.4:p.Phe1003Leu
XM_005258809.2:c.2972-315T>C	XP_005258866.1:n.2972-315T>C
XM_011526837.1:c.2992T>C	XP_011525139.1:p.Phe998Leu
XM_011526838.1:c.2971+382T>C	XP_011525140.1:n.2971+382T>C
XM_011526839.1:c.2656T>C	XP_011525141.1:p.Phe886Leu
XM_011526840.1:c.1999T>C	XP_011525142.1:p.Phe667Leu
XM_011526841.1:c.1585T>C	XP_011525143.1:p.Phe529Leu
XM_011526842.1:c.1438T>C	XP_011525144.1:p.Phe480Leu
XM_011526843.1:c.754T>C	XP_011525145.1:p.Phe252Leu
XM_011526844.1:c.754T>C	XP_011525146.1:p.Phe252Leu
XM_011526840.2:c.1999T>C	XP_011525142.1:p.Phe667Leu
XM_011526841.2:c.1585T>C	XP_011525143.1:p.Phe529Leu
XM_011526844.2:c.754T>C	XP_011525146.1:p.Phe252Leu
XM_017026665.1:c.3007T>C	XP_016882154.1:p.Phe1003Leu
NM_001083961.2:c.3007T>C MANE Select	NP_001077430.1:p.Phe1003Leu
NM_173636.5:c.3007T>C	NP_775907.4:p.Phe1003Leu