Canonical Allele Identifier: CA405450819

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593036C>T (hg19) ; chr19:g.36102134C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102134C>T , CM000681.2:g.36102134C>T	GRCh38
NC_000019.9:g.36593036C>T , CM000681.1:g.36593036C>T	GRCh37
NC_000019.8:g.41284876C>T	NCBI36
NG_028101.1:g.52254C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3203C>T	ENSP00000270301.6:p.Thr1068Ile
ENST00000401500.7:c.3203C>T MANE Select	ENSP00000384792.1:p.Thr1068Ile
ENST00000587391.6:c.*2478C>T	ENSP00000465525.1:n.*2478C>T
ENST00000679357.1:c.993C>T
ENST00000679422.1:c.882C>T
ENST00000679682.1:c.3188C>T	ENSP00000506226.1:p.Thr1063Ile
ENST00000679714.1:c.3197C>T	ENSP00000506627.1:p.Thr1066Ile
ENST00000679757.1:c.2852C>T	ENSP00000505158.1:p.Thr951Ile
ENST00000679858.1:c.*2585C>T	ENSP00000505655.1:n.*2585C>T
ENST00000680211.1:c.-197C>T	ENSP00000506102.1:n.-197C>T
ENST00000680349.1:n.1186C>T
ENST00000680403.1:c.3203C>T	ENSP00000505677.1:p.Thr1068Ile
ENST00000680564.1:c.2972-603C>T	ENSP00000505582.1:n.2972-603C>T
ENST00000680590.1:c.*1598C>T	ENSP00000505350.1:n.*1598C>T
ENST00000680739.1:c.121C>T
ENST00000680773.1:n.1119C>T
ENST00000680806.1:c.*1921C>T	ENSP00000506418.1:n.*1921C>T
ENST00000680997.1:n.550C>T
ENST00000681088.1:c.865C>T
ENST00000681608.1:n.151C>T
ENST00000681625.1:c.*535C>T	ENSP00000505555.1:n.*535C>T
ENST00000270301.11:c.3203C>T	ENSP00000270301.6:p.Thr1068Ile
ENST00000401500.6:c.3203C>T	ENSP00000384792.1:p.Thr1068Ile
ENST00000587391.5:c.*2478C>T	ENSP00000465525.1:n.*2478C>T
NM_001083961.1:c.3203C>T	NP_001077430.1:p.Thr1068Ile
NM_173636.4:c.3203C>T	NP_775907.4:p.Thr1068Ile
XM_005258809.2:c.3092C>T	XP_005258866.1:p.Thr1031Ile
XM_011526837.1:c.3188C>T	XP_011525139.1:p.Thr1063Ile
XM_011526838.1:c.2972-603C>T	XP_011525140.1:n.2972-603C>T
XM_011526839.1:c.2852C>T	XP_011525141.1:p.Thr951Ile
XM_011526840.1:c.2195C>T	XP_011525142.1:p.Thr732Ile
XM_011526841.1:c.1781C>T	XP_011525143.1:p.Thr594Ile
XM_011526842.1:c.1634C>T	XP_011525144.1:p.Thr545Ile
XM_011526843.1:c.950C>T	XP_011525145.1:p.Thr317Ile
XM_011526844.1:c.950C>T	XP_011525146.1:p.Thr317Ile
XM_011526840.2:c.2195C>T	XP_011525142.1:p.Thr732Ile
XM_011526841.2:c.1781C>T	XP_011525143.1:p.Thr594Ile
XM_011526844.2:c.950C>T	XP_011525146.1:p.Thr317Ile
XM_017026665.1:c.3203C>T	XP_016882154.1:p.Thr1068Ile
NM_001083961.2:c.3203C>T MANE Select	NP_001077430.1:p.Thr1068Ile
NM_173636.5:c.3203C>T	NP_775907.4:p.Thr1068Ile