Canonical Allele Identifier: CA507107562

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36592992T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102090T>G , CM000681.2:g.36102090T>G	GRCh38
NC_000019.9:g.36592992T>G , CM000681.1:g.36592992T>G	GRCh37
NC_000019.8:g.41284832T>G	NCBI36
NG_028101.1:g.52210T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3159T>G	ENSP00000270301.6:p.Thr1053=
ENST00000401500.7:c.3159T>G MANE Select	ENSP00000384792.1:p.Thr1053=
ENST00000587391.6:c.*2434T>G	ENSP00000465525.1:n.*2434T>G
ENST00000679357.1:c.949T>G
ENST00000679422.1:c.838T>G
ENST00000679682.1:c.3144T>G	ENSP00000506226.1:p.Thr1048=
ENST00000679714.1:c.3153T>G	ENSP00000506627.1:p.Thr1051=
ENST00000679757.1:c.2808T>G	ENSP00000505158.1:p.Thr936=
ENST00000679858.1:c.*2541T>G	ENSP00000505655.1:n.*2541T>G
ENST00000680211.1:c.-241T>G	ENSP00000506102.1:n.-241T>G
ENST00000680349.1:n.1142T>G
ENST00000680403.1:c.3159T>G	ENSP00000505677.1:p.Thr1053=
ENST00000680564.1:c.2972-647T>G	ENSP00000505582.1:n.2972-647T>G
ENST00000680590.1:c.*1554T>G	ENSP00000505350.1:n.*1554T>G
ENST00000680739.1:c.77T>G
ENST00000680773.1:n.1075T>G
ENST00000680806.1:c.*1877T>G	ENSP00000506418.1:n.*1877T>G
ENST00000680997.1:n.506T>G
ENST00000681088.1:c.821T>G
ENST00000681608.1:n.107T>G
ENST00000681625.1:c.*491T>G	ENSP00000505555.1:n.*491T>G
ENST00000270301.11:c.3159T>G	ENSP00000270301.6:p.Thr1053=
ENST00000401500.6:c.3159T>G	ENSP00000384792.1:p.Thr1053=
ENST00000587391.5:c.*2434T>G	ENSP00000465525.1:n.*2434T>G
NM_001083961.1:c.3159T>G	NP_001077430.1:p.Thr1053=
NM_173636.4:c.3159T>G	NP_775907.4:p.Thr1053=
XM_005258809.2:c.3048T>G	XP_005258866.1:p.Thr1016=
XM_011526837.1:c.3144T>G	XP_011525139.1:p.Thr1048=
XM_011526838.1:c.2972-647T>G	XP_011525140.1:n.2972-647T>G
XM_011526839.1:c.2808T>G	XP_011525141.1:p.Thr936=
XM_011526840.1:c.2151T>G	XP_011525142.1:p.Thr717=
XM_011526841.1:c.1737T>G	XP_011525143.1:p.Thr579=
XM_011526842.1:c.1590T>G	XP_011525144.1:p.Thr530=
XM_011526843.1:c.906T>G	XP_011525145.1:p.Thr302=
XM_011526844.1:c.906T>G	XP_011525146.1:p.Thr302=
XM_011526840.2:c.2151T>G	XP_011525142.1:p.Thr717=
XM_011526841.2:c.1737T>G	XP_011525143.1:p.Thr579=
XM_011526844.2:c.906T>G	XP_011525146.1:p.Thr302=
XM_017026665.1:c.3159T>G	XP_016882154.1:p.Thr1053=
NM_001083961.2:c.3159T>G MANE Select	NP_001077430.1:p.Thr1053=
NM_173636.5:c.3159T>G	NP_775907.4:p.Thr1053=