Canonical Allele Identifier: CA405452729

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593870C>G (hg19) ; chr19:g.36102968C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102968C>G , CM000681.2:g.36102968C>G	GRCh38
NC_000019.9:g.36593870C>G , CM000681.1:g.36593870C>G	GRCh37
NC_000019.8:g.41285710C>G	NCBI36
NG_028101.1:g.53088C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3341C>G	ENSP00000270301.6:p.Pro1114Arg
ENST00000401500.7:c.3356C>G MANE Select	ENSP00000384792.1:p.Pro1119Arg
ENST00000587391.6:c.*3216C>G	ENSP00000465525.1:n.*3216C>G
ENST00000679357.1:c.1436C>G
ENST00000679598.1:c.121C>G
ENST00000679682.1:c.3341C>G	ENSP00000506226.1:p.Pro1114Arg
ENST00000679714.1:c.3350C>G	ENSP00000506627.1:p.Pro1117Arg
ENST00000679757.1:c.3005C>G	ENSP00000505158.1:p.Pro1002Arg
ENST00000679858.1:c.*2738C>G	ENSP00000505655.1:n.*2738C>G
ENST00000680211.1:c.-44C>G	ENSP00000506102.1:n.-44C>G
ENST00000680280.1:n.643C>G
ENST00000680349.1:n.1924C>G
ENST00000680403.1:c.3341C>G	ENSP00000505677.1:p.Pro1114Arg
ENST00000680564.1:c.3107C>G	ENSP00000505582.1:p.Pro1036Arg
ENST00000680590.1:c.*1736C>G	ENSP00000505350.1:n.*1736C>G
ENST00000680597.1:c.121C>G
ENST00000680739.1:c.371C>G
ENST00000680773.1:n.1857C>G
ENST00000680806.1:c.*2659C>G	ENSP00000506418.1:n.*2659C>G
ENST00000680997.1:n.1288C>G
ENST00000681608.1:n.985C>G
ENST00000681625.1:c.*688C>G	ENSP00000505555.1:n.*688C>G
ENST00000681648.1:n.655C>G
ENST00000270301.11:c.3341C>G	ENSP00000270301.6:p.Pro1114Arg
ENST00000401500.6:c.3356C>G	ENSP00000384792.1:p.Pro1119Arg
ENST00000587391.5:c.*3216C>G	ENSP00000465525.1:n.*3216C>G
NM_001083961.1:c.3356C>G	NP_001077430.1:p.Pro1119Arg
NM_173636.4:c.3341C>G	NP_775907.4:p.Pro1114Arg
XM_005258809.2:c.3245C>G	XP_005258866.1:p.Pro1082Arg
XM_011526837.1:c.3341C>G	XP_011525139.1:p.Pro1114Arg
XM_011526838.1:c.3107C>G	XP_011525140.1:p.Pro1036Arg
XM_011526839.1:c.3005C>G	XP_011525141.1:p.Pro1002Arg
XM_011526840.1:c.2348C>G	XP_011525142.1:p.Pro783Arg
XM_011526841.1:c.1934C>G	XP_011525143.1:p.Pro645Arg
XM_011526842.1:c.1787C>G	XP_011525144.1:p.Pro596Arg
XM_011526843.1:c.1103C>G	XP_011525145.1:p.Pro368Arg
XM_011526844.1:c.1103C>G	XP_011525146.1:p.Pro368Arg
XM_011526840.2:c.2348C>G	XP_011525142.1:p.Pro783Arg
XM_011526841.2:c.1934C>G	XP_011525143.1:p.Pro645Arg
XM_011526844.2:c.1103C>G	XP_011525146.1:p.Pro368Arg
XM_017026665.1:c.3356C>G	XP_016882154.1:p.Pro1119Arg
NM_001083961.2:c.3356C>G MANE Select	NP_001077430.1:p.Pro1119Arg
NM_173636.5:c.3341C>G	NP_775907.4:p.Pro1114Arg