Canonical Allele Identifier: CA307843067

Gene: WDR62

Linked Data

• dbSNP Id: rs376026671
• gnomAD v2: 19-36595475-G-T
• gnomAD v4: 19-36104573-G-T
• MyVariant Identifiers: chr19:g.36595475G>T (hg19) ; chr19:g.36104573G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104573G>T , CM000681.2:g.36104573G>T	GRCh38
NC_000019.9:g.36595475G>T , CM000681.1:g.36595475G>T	GRCh37
NC_000019.8:g.41287315G>T	NCBI36
NG_028101.1:g.54693G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4194G>T	ENSP00000270301.6:p.Pro1398=
ENST00000401500.7:c.4209G>T MANE Select	ENSP00000384792.1:p.Pro1403=
ENST00000587391.6:c.*4069G>T	ENSP00000465525.1:n.*4069G>T
ENST00000679357.1:c.2289G>T
ENST00000679598.1:c.954G>T
ENST00000679682.1:c.4194G>T	ENSP00000506226.1:p.Pro1398=
ENST00000679714.1:c.4203G>T	ENSP00000506627.1:p.Pro1401=
ENST00000679757.1:c.3858G>T	ENSP00000505158.1:p.Pro1286=
ENST00000679858.1:c.*3591G>T	ENSP00000505655.1:n.*3591G>T
ENST00000680211.1:c.810G>T	ENSP00000506102.1:p.Pro270=
ENST00000680280.1:n.1712G>T
ENST00000680349.1:n.2858G>T
ENST00000680403.1:c.4194G>T	ENSP00000505677.1:p.Pro1398=
ENST00000680564.1:c.3960G>T	ENSP00000505582.1:p.Pro1320=
ENST00000680590.1:c.*2589G>T	ENSP00000505350.1:n.*2589G>T
ENST00000680597.1:c.942G>T
ENST00000680739.1:c.1224G>T
ENST00000680773.1:n.2710G>T
ENST00000680806.1:c.*3512G>T	ENSP00000506418.1:n.*3512G>T
ENST00000680997.1:n.2141G>T
ENST00000681608.1:n.2054G>T
ENST00000681625.1:c.*1541G>T	ENSP00000505555.1:n.*1541G>T
ENST00000681648.1:n.2260G>T
ENST00000270301.11:c.4194G>T	ENSP00000270301.6:p.Pro1398=
ENST00000401500.6:c.4209G>T	ENSP00000384792.1:p.Pro1403=
ENST00000587391.5:c.*4069G>T	ENSP00000465525.1:n.*4069G>T
NM_001083961.1:c.4209G>T	NP_001077430.1:p.Pro1403=
NM_173636.4:c.4194G>T	NP_775907.4:p.Pro1398=
XM_005258809.2:c.4098G>T	XP_005258866.1:p.Pro1366=
XM_011526837.1:c.4194G>T	XP_011525139.1:p.Pro1398=
XM_011526838.1:c.3960G>T	XP_011525140.1:p.Pro1320=
XM_011526839.1:c.3858G>T	XP_011525141.1:p.Pro1286=
XM_011526840.1:c.3201G>T	XP_011525142.1:p.Pro1067=
XM_011526841.1:c.2787G>T	XP_011525143.1:p.Pro929=
XM_011526842.1:c.2640G>T	XP_011525144.1:p.Pro880=
XM_011526843.1:c.1956G>T	XP_011525145.1:p.Pro652=
XM_011526844.1:c.1956G>T	XP_011525146.1:p.Pro652=
XM_011526840.2:c.3201G>T	XP_011525142.1:p.Pro1067=
XM_011526841.2:c.2787G>T	XP_011525143.1:p.Pro929=
XM_011526844.2:c.1956G>T	XP_011525146.1:p.Pro652=
XM_017026665.1:c.4209G>T	XP_016882154.1:p.Pro1403=
NM_001083961.2:c.4209G>T MANE Select	NP_001077430.1:p.Pro1403=
NM_173636.5:c.4194G>T	NP_775907.4:p.Pro1398=