Canonical Allele Identifier: CA405452039

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593717C>A (hg19) ; chr19:g.36102815C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102815C>A , CM000681.2:g.36102815C>A	GRCh38
NC_000019.9:g.36593717C>A , CM000681.1:g.36593717C>A	GRCh37
NC_000019.8:g.41285557C>A	NCBI36
NG_028101.1:g.52935C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3284C>A	ENSP00000270301.6:p.Ser1095Tyr
ENST00000401500.7:c.3299C>A MANE Select	ENSP00000384792.1:p.Ser1100Tyr
ENST00000587391.6:c.*3159C>A	ENSP00000465525.1:n.*3159C>A
ENST00000679357.1:c.1379C>A
ENST00000679598.1:c.64C>A
ENST00000679682.1:c.3284C>A	ENSP00000506226.1:p.Ser1095Tyr
ENST00000679714.1:c.3293C>A	ENSP00000506627.1:p.Ser1098Tyr
ENST00000679757.1:c.2948C>A	ENSP00000505158.1:p.Ser983Tyr
ENST00000679858.1:c.*2681C>A	ENSP00000505655.1:n.*2681C>A
ENST00000680211.1:c.-101C>A	ENSP00000506102.1:n.-101C>A
ENST00000680280.1:n.586C>A
ENST00000680349.1:n.1867C>A
ENST00000680403.1:c.3284C>A	ENSP00000505677.1:p.Ser1095Tyr
ENST00000680564.1:c.3050C>A	ENSP00000505582.1:p.Ser1017Tyr
ENST00000680590.1:c.*1679C>A	ENSP00000505350.1:n.*1679C>A
ENST00000680597.1:c.64C>A
ENST00000680739.1:c.314C>A
ENST00000680773.1:n.1800C>A
ENST00000680806.1:c.*2602C>A	ENSP00000506418.1:n.*2602C>A
ENST00000680997.1:n.1231C>A
ENST00000681608.1:n.832C>A
ENST00000681625.1:c.*631C>A	ENSP00000505555.1:n.*631C>A
ENST00000681648.1:n.598C>A
ENST00000270301.11:c.3284C>A	ENSP00000270301.6:p.Ser1095Tyr
ENST00000401500.6:c.3299C>A	ENSP00000384792.1:p.Ser1100Tyr
ENST00000587391.5:c.*3159C>A	ENSP00000465525.1:n.*3159C>A
NM_001083961.1:c.3299C>A	NP_001077430.1:p.Ser1100Tyr
NM_173636.4:c.3284C>A	NP_775907.4:p.Ser1095Tyr
XM_005258809.2:c.3188C>A	XP_005258866.1:p.Ser1063Tyr
XM_011526837.1:c.3284C>A	XP_011525139.1:p.Ser1095Tyr
XM_011526838.1:c.3050C>A	XP_011525140.1:p.Ser1017Tyr
XM_011526839.1:c.2948C>A	XP_011525141.1:p.Ser983Tyr
XM_011526840.1:c.2291C>A	XP_011525142.1:p.Ser764Tyr
XM_011526841.1:c.1877C>A	XP_011525143.1:p.Ser626Tyr
XM_011526842.1:c.1730C>A	XP_011525144.1:p.Ser577Tyr
XM_011526843.1:c.1046C>A	XP_011525145.1:p.Ser349Tyr
XM_011526844.1:c.1046C>A	XP_011525146.1:p.Ser349Tyr
XM_011526840.2:c.2291C>A	XP_011525142.1:p.Ser764Tyr
XM_011526841.2:c.1877C>A	XP_011525143.1:p.Ser626Tyr
XM_011526844.2:c.1046C>A	XP_011525146.1:p.Ser349Tyr
XM_017026665.1:c.3299C>A	XP_016882154.1:p.Ser1100Tyr
NM_001083961.2:c.3299C>A MANE Select	NP_001077430.1:p.Ser1100Tyr
NM_173636.5:c.3284C>A	NP_775907.4:p.Ser1095Tyr