Canonical Allele Identifier: CA405450006

Gene: WDR62

Linked Data

• dbSNP Id: rs1973381279
• gnomAD v3: 19-36102035-A-T
• gnomAD v4: 19-36102035-A-T
• MyVariant Identifiers: chr19:g.36592937A>T (hg19) ; chr19:g.36102035A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102035A>T , CM000681.2:g.36102035A>T	GRCh38
NC_000019.9:g.36592937A>T , CM000681.1:g.36592937A>T	GRCh37
NC_000019.8:g.41284777A>T	NCBI36
NG_028101.1:g.52155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3104A>T	ENSP00000270301.6:p.Asp1035Val
ENST00000401500.7:c.3104A>T MANE Select	ENSP00000384792.1:p.Asp1035Val
ENST00000587391.6:c.*2379A>T	ENSP00000465525.1:n.*2379A>T
ENST00000679357.1:c.894A>T
ENST00000679422.1:c.783A>T
ENST00000679682.1:c.3089A>T	ENSP00000506226.1:p.Asp1030Val
ENST00000679714.1:c.3098A>T	ENSP00000506627.1:p.Asp1033Val
ENST00000679757.1:c.2753A>T	ENSP00000505158.1:p.Asp918Val
ENST00000679858.1:c.*2486A>T	ENSP00000505655.1:n.*2486A>T
ENST00000680211.1:c.-296A>T	ENSP00000506102.1:n.-296A>T
ENST00000680349.1:n.1087A>T
ENST00000680403.1:c.3104A>T	ENSP00000505677.1:p.Asp1035Val
ENST00000680564.1:c.2972-702A>T	ENSP00000505582.1:n.2972-702A>T
ENST00000680590.1:c.*1499A>T	ENSP00000505350.1:n.*1499A>T
ENST00000680739.1:c.22A>T
ENST00000680773.1:n.1020A>T
ENST00000680806.1:c.*1822A>T	ENSP00000506418.1:n.*1822A>T
ENST00000680997.1:n.451A>T
ENST00000681088.1:c.766A>T
ENST00000681608.1:n.52A>T
ENST00000681625.1:c.*436A>T	ENSP00000505555.1:n.*436A>T
ENST00000270301.11:c.3104A>T	ENSP00000270301.6:p.Asp1035Val
ENST00000401500.6:c.3104A>T	ENSP00000384792.1:p.Asp1035Val
ENST00000587391.5:c.*2379A>T	ENSP00000465525.1:n.*2379A>T
NM_001083961.1:c.3104A>T	NP_001077430.1:p.Asp1035Val
NM_173636.4:c.3104A>T	NP_775907.4:p.Asp1035Val
XM_005258809.2:c.2993A>T	XP_005258866.1:p.Asp998Val
XM_011526837.1:c.3089A>T	XP_011525139.1:p.Asp1030Val
XM_011526838.1:c.2972-702A>T	XP_011525140.1:n.2972-702A>T
XM_011526839.1:c.2753A>T	XP_011525141.1:p.Asp918Val
XM_011526840.1:c.2096A>T	XP_011525142.1:p.Asp699Val
XM_011526841.1:c.1682A>T	XP_011525143.1:p.Asp561Val
XM_011526842.1:c.1535A>T	XP_011525144.1:p.Asp512Val
XM_011526843.1:c.851A>T	XP_011525145.1:p.Asp284Val
XM_011526844.1:c.851A>T	XP_011525146.1:p.Asp284Val
XM_011526840.2:c.2096A>T	XP_011525142.1:p.Asp699Val
XM_011526841.2:c.1682A>T	XP_011525143.1:p.Asp561Val
XM_011526844.2:c.851A>T	XP_011525146.1:p.Asp284Val
XM_017026665.1:c.3104A>T	XP_016882154.1:p.Asp1035Val
NM_001083961.2:c.3104A>T MANE Select	NP_001077430.1:p.Asp1035Val
NM_173636.5:c.3104A>T	NP_775907.4:p.Asp1035Val