Canonical Allele Identifier: CA405452037

Gene: WDR62

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3284C>G	ENSP00000270301.6:p.Ser1095Cys
ENST00000401500.7:c.3299C>G MANE Select	ENSP00000384792.1:p.Ser1100Cys
ENST00000587391.6:c.*3159C>G	ENSP00000465525.1:n.*3159C>G
ENST00000679357.1:c.1379C>G
ENST00000679598.1:c.64C>G
ENST00000679682.1:c.3284C>G	ENSP00000506226.1:p.Ser1095Cys
ENST00000679714.1:c.3293C>G	ENSP00000506627.1:p.Ser1098Cys
ENST00000679757.1:c.2948C>G	ENSP00000505158.1:p.Ser983Cys
ENST00000679858.1:c.*2681C>G	ENSP00000505655.1:n.*2681C>G
ENST00000680211.1:c.-101C>G	ENSP00000506102.1:n.-101C>G
ENST00000680280.1:n.586C>G
ENST00000680349.1:n.1867C>G
ENST00000680403.1:c.3284C>G	ENSP00000505677.1:p.Ser1095Cys
ENST00000680564.1:c.3050C>G	ENSP00000505582.1:p.Ser1017Cys
ENST00000680590.1:c.*1679C>G	ENSP00000505350.1:n.*1679C>G
ENST00000680597.1:c.64C>G
ENST00000680739.1:c.314C>G
ENST00000680773.1:n.1800C>G
ENST00000680806.1:c.*2602C>G	ENSP00000506418.1:n.*2602C>G
ENST00000680997.1:n.1231C>G
ENST00000681608.1:n.832C>G
ENST00000681625.1:c.*631C>G	ENSP00000505555.1:n.*631C>G
ENST00000681648.1:n.598C>G
ENST00000270301.11:c.3284C>G	ENSP00000270301.6:p.Ser1095Cys
ENST00000401500.6:c.3299C>G	ENSP00000384792.1:p.Ser1100Cys
ENST00000587391.5:c.*3159C>G	ENSP00000465525.1:n.*3159C>G
NM_001083961.1:c.3299C>G	NP_001077430.1:p.Ser1100Cys
NM_173636.4:c.3284C>G	NP_775907.4:p.Ser1095Cys
XM_005258809.2:c.3188C>G	XP_005258866.1:p.Ser1063Cys
XM_011526837.1:c.3284C>G	XP_011525139.1:p.Ser1095Cys
XM_011526838.1:c.3050C>G	XP_011525140.1:p.Ser1017Cys
XM_011526839.1:c.2948C>G	XP_011525141.1:p.Ser983Cys
XM_011526840.1:c.2291C>G	XP_011525142.1:p.Ser764Cys
XM_011526841.1:c.1877C>G	XP_011525143.1:p.Ser626Cys
XM_011526842.1:c.1730C>G	XP_011525144.1:p.Ser577Cys
XM_011526843.1:c.1046C>G	XP_011525145.1:p.Ser349Cys
XM_011526844.1:c.1046C>G	XP_011525146.1:p.Ser349Cys
XM_011526840.2:c.2291C>G	XP_011525142.1:p.Ser764Cys
XM_011526841.2:c.1877C>G	XP_011525143.1:p.Ser626Cys
XM_011526844.2:c.1046C>G	XP_011525146.1:p.Ser349Cys
XM_017026665.1:c.3299C>G	XP_016882154.1:p.Ser1100Cys
NM_001083961.2:c.3299C>G MANE Select	NP_001077430.1:p.Ser1100Cys
NM_173636.5:c.3284C>G	NP_775907.4:p.Ser1095Cys