Canonical Allele Identifier: CA405452196

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593741A>T (hg19) ; chr19:g.36102839A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102839A>T , CM000681.2:g.36102839A>T	GRCh38
NC_000019.9:g.36593741A>T , CM000681.1:g.36593741A>T	GRCh37
NC_000019.8:g.41285581A>T	NCBI36
NG_028101.1:g.52959A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3308A>T	ENSP00000270301.6:p.Gln1103Leu
ENST00000401500.7:c.3323A>T MANE Select	ENSP00000384792.1:p.Gln1108Leu
ENST00000587391.6:c.*3183A>T	ENSP00000465525.1:n.*3183A>T
ENST00000679357.1:c.1403A>T
ENST00000679598.1:c.88A>T
ENST00000679682.1:c.3308A>T	ENSP00000506226.1:p.Gln1103Leu
ENST00000679714.1:c.3317A>T	ENSP00000506627.1:p.Gln1106Leu
ENST00000679757.1:c.2972A>T	ENSP00000505158.1:p.Gln991Leu
ENST00000679858.1:c.*2705A>T	ENSP00000505655.1:n.*2705A>T
ENST00000680211.1:c.-77A>T	ENSP00000506102.1:n.-77A>T
ENST00000680280.1:n.610A>T
ENST00000680349.1:n.1891A>T
ENST00000680403.1:c.3308A>T	ENSP00000505677.1:p.Gln1103Leu
ENST00000680564.1:c.3074A>T	ENSP00000505582.1:p.Gln1025Leu
ENST00000680590.1:c.*1703A>T	ENSP00000505350.1:n.*1703A>T
ENST00000680597.1:c.88A>T
ENST00000680739.1:c.338A>T
ENST00000680773.1:n.1824A>T
ENST00000680806.1:c.*2626A>T	ENSP00000506418.1:n.*2626A>T
ENST00000680997.1:n.1255A>T
ENST00000681608.1:n.856A>T
ENST00000681625.1:c.*655A>T	ENSP00000505555.1:n.*655A>T
ENST00000681648.1:n.622A>T
ENST00000270301.11:c.3308A>T	ENSP00000270301.6:p.Gln1103Leu
ENST00000401500.6:c.3323A>T	ENSP00000384792.1:p.Gln1108Leu
ENST00000587391.5:c.*3183A>T	ENSP00000465525.1:n.*3183A>T
NM_001083961.1:c.3323A>T	NP_001077430.1:p.Gln1108Leu
NM_173636.4:c.3308A>T	NP_775907.4:p.Gln1103Leu
XM_005258809.2:c.3212A>T	XP_005258866.1:p.Gln1071Leu
XM_011526837.1:c.3308A>T	XP_011525139.1:p.Gln1103Leu
XM_011526838.1:c.3074A>T	XP_011525140.1:p.Gln1025Leu
XM_011526839.1:c.2972A>T	XP_011525141.1:p.Gln991Leu
XM_011526840.1:c.2315A>T	XP_011525142.1:p.Gln772Leu
XM_011526841.1:c.1901A>T	XP_011525143.1:p.Gln634Leu
XM_011526842.1:c.1754A>T	XP_011525144.1:p.Gln585Leu
XM_011526843.1:c.1070A>T	XP_011525145.1:p.Gln357Leu
XM_011526844.1:c.1070A>T	XP_011525146.1:p.Gln357Leu
XM_011526840.2:c.2315A>T	XP_011525142.1:p.Gln772Leu
XM_011526841.2:c.1901A>T	XP_011525143.1:p.Gln634Leu
XM_011526844.2:c.1070A>T	XP_011525146.1:p.Gln357Leu
XM_017026665.1:c.3323A>T	XP_016882154.1:p.Gln1108Leu
NM_001083961.2:c.3323A>T MANE Select	NP_001077430.1:p.Gln1108Leu
NM_173636.5:c.3308A>T	NP_775907.4:p.Gln1103Leu