Canonical Allele Identifier: CA405450804

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593035A>T (hg19) ; chr19:g.36102133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102133A>T , CM000681.2:g.36102133A>T	GRCh38
NC_000019.9:g.36593035A>T , CM000681.1:g.36593035A>T	GRCh37
NC_000019.8:g.41284875A>T	NCBI36
NG_028101.1:g.52253A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3202A>T	ENSP00000270301.6:p.Thr1068Ser
ENST00000401500.7:c.3202A>T MANE Select	ENSP00000384792.1:p.Thr1068Ser
ENST00000587391.6:c.*2477A>T	ENSP00000465525.1:n.*2477A>T
ENST00000679357.1:c.992A>T
ENST00000679422.1:c.881A>T
ENST00000679682.1:c.3187A>T	ENSP00000506226.1:p.Thr1063Ser
ENST00000679714.1:c.3196A>T	ENSP00000506627.1:p.Thr1066Ser
ENST00000679757.1:c.2851A>T	ENSP00000505158.1:p.Thr951Ser
ENST00000679858.1:c.*2584A>T	ENSP00000505655.1:n.*2584A>T
ENST00000680211.1:c.-198A>T	ENSP00000506102.1:n.-198A>T
ENST00000680349.1:n.1185A>T
ENST00000680403.1:c.3202A>T	ENSP00000505677.1:p.Thr1068Ser
ENST00000680564.1:c.2972-604A>T	ENSP00000505582.1:n.2972-604A>T
ENST00000680590.1:c.*1597A>T	ENSP00000505350.1:n.*1597A>T
ENST00000680739.1:c.120A>T
ENST00000680773.1:n.1118A>T
ENST00000680806.1:c.*1920A>T	ENSP00000506418.1:n.*1920A>T
ENST00000680997.1:n.549A>T
ENST00000681088.1:c.864A>T
ENST00000681608.1:n.150A>T
ENST00000681625.1:c.*534A>T	ENSP00000505555.1:n.*534A>T
ENST00000270301.11:c.3202A>T	ENSP00000270301.6:p.Thr1068Ser
ENST00000401500.6:c.3202A>T	ENSP00000384792.1:p.Thr1068Ser
ENST00000587391.5:c.*2477A>T	ENSP00000465525.1:n.*2477A>T
NM_001083961.1:c.3202A>T	NP_001077430.1:p.Thr1068Ser
NM_173636.4:c.3202A>T	NP_775907.4:p.Thr1068Ser
XM_005258809.2:c.3091A>T	XP_005258866.1:p.Thr1031Ser
XM_011526837.1:c.3187A>T	XP_011525139.1:p.Thr1063Ser
XM_011526838.1:c.2972-604A>T	XP_011525140.1:n.2972-604A>T
XM_011526839.1:c.2851A>T	XP_011525141.1:p.Thr951Ser
XM_011526840.1:c.2194A>T	XP_011525142.1:p.Thr732Ser
XM_011526841.1:c.1780A>T	XP_011525143.1:p.Thr594Ser
XM_011526842.1:c.1633A>T	XP_011525144.1:p.Thr545Ser
XM_011526843.1:c.949A>T	XP_011525145.1:p.Thr317Ser
XM_011526844.1:c.949A>T	XP_011525146.1:p.Thr317Ser
XM_011526840.2:c.2194A>T	XP_011525142.1:p.Thr732Ser
XM_011526841.2:c.1780A>T	XP_011525143.1:p.Thr594Ser
XM_011526844.2:c.949A>T	XP_011525146.1:p.Thr317Ser
XM_017026665.1:c.3202A>T	XP_016882154.1:p.Thr1068Ser
NM_001083961.2:c.3202A>T MANE Select	NP_001077430.1:p.Thr1068Ser
NM_173636.5:c.3202A>T	NP_775907.4:p.Thr1068Ser