Canonical Allele Identifier: CA405452656

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593864T>C (hg19) ; chr19:g.36102962T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102962T>C , CM000681.2:g.36102962T>C	GRCh38
NC_000019.9:g.36593864T>C , CM000681.1:g.36593864T>C	GRCh37
NC_000019.8:g.41285704T>C	NCBI36
NG_028101.1:g.53082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3335T>C	ENSP00000270301.6:p.Phe1112Ser
ENST00000401500.7:c.3350T>C MANE Select	ENSP00000384792.1:p.Phe1117Ser
ENST00000587391.6:c.*3210T>C	ENSP00000465525.1:n.*3210T>C
ENST00000679357.1:c.1430T>C
ENST00000679598.1:c.115T>C
ENST00000679682.1:c.3335T>C	ENSP00000506226.1:p.Phe1112Ser
ENST00000679714.1:c.3344T>C	ENSP00000506627.1:p.Phe1115Ser
ENST00000679757.1:c.2999T>C	ENSP00000505158.1:p.Phe1000Ser
ENST00000679858.1:c.*2732T>C	ENSP00000505655.1:n.*2732T>C
ENST00000680211.1:c.-50T>C	ENSP00000506102.1:n.-50T>C
ENST00000680280.1:n.637T>C
ENST00000680349.1:n.1918T>C
ENST00000680403.1:c.3335T>C	ENSP00000505677.1:p.Phe1112Ser
ENST00000680564.1:c.3101T>C	ENSP00000505582.1:p.Phe1034Ser
ENST00000680590.1:c.*1730T>C	ENSP00000505350.1:n.*1730T>C
ENST00000680597.1:c.115T>C
ENST00000680739.1:c.365T>C
ENST00000680773.1:n.1851T>C
ENST00000680806.1:c.*2653T>C	ENSP00000506418.1:n.*2653T>C
ENST00000680997.1:n.1282T>C
ENST00000681608.1:n.979T>C
ENST00000681625.1:c.*682T>C	ENSP00000505555.1:n.*682T>C
ENST00000681648.1:n.649T>C
ENST00000270301.11:c.3335T>C	ENSP00000270301.6:p.Phe1112Ser
ENST00000401500.6:c.3350T>C	ENSP00000384792.1:p.Phe1117Ser
ENST00000587391.5:c.*3210T>C	ENSP00000465525.1:n.*3210T>C
NM_001083961.1:c.3350T>C	NP_001077430.1:p.Phe1117Ser
NM_173636.4:c.3335T>C	NP_775907.4:p.Phe1112Ser
XM_005258809.2:c.3239T>C	XP_005258866.1:p.Phe1080Ser
XM_011526837.1:c.3335T>C	XP_011525139.1:p.Phe1112Ser
XM_011526838.1:c.3101T>C	XP_011525140.1:p.Phe1034Ser
XM_011526839.1:c.2999T>C	XP_011525141.1:p.Phe1000Ser
XM_011526840.1:c.2342T>C	XP_011525142.1:p.Phe781Ser
XM_011526841.1:c.1928T>C	XP_011525143.1:p.Phe643Ser
XM_011526842.1:c.1781T>C	XP_011525144.1:p.Phe594Ser
XM_011526843.1:c.1097T>C	XP_011525145.1:p.Phe366Ser
XM_011526844.1:c.1097T>C	XP_011525146.1:p.Phe366Ser
XM_011526840.2:c.2342T>C	XP_011525142.1:p.Phe781Ser
XM_011526841.2:c.1928T>C	XP_011525143.1:p.Phe643Ser
XM_011526844.2:c.1097T>C	XP_011525146.1:p.Phe366Ser
XM_017026665.1:c.3350T>C	XP_016882154.1:p.Phe1117Ser
NM_001083961.2:c.3350T>C MANE Select	NP_001077430.1:p.Phe1117Ser
NM_173636.5:c.3335T>C	NP_775907.4:p.Phe1112Ser