Canonical Allele Identifier: CA405449993

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102034-G-C
• MyVariant Identifiers: chr19:g.36592936G>C (hg19) ; chr19:g.36102034G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102034G>C , CM000681.2:g.36102034G>C	GRCh38
NC_000019.9:g.36592936G>C , CM000681.1:g.36592936G>C	GRCh37
NC_000019.8:g.41284776G>C	NCBI36
NG_028101.1:g.52154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3103G>C	ENSP00000270301.6:p.Asp1035His
ENST00000401500.7:c.3103G>C MANE Select	ENSP00000384792.1:p.Asp1035His
ENST00000587391.6:c.*2378G>C	ENSP00000465525.1:n.*2378G>C
ENST00000679357.1:c.893G>C
ENST00000679422.1:c.782G>C
ENST00000679682.1:c.3088G>C	ENSP00000506226.1:p.Asp1030His
ENST00000679714.1:c.3097G>C	ENSP00000506627.1:p.Asp1033His
ENST00000679757.1:c.2752G>C	ENSP00000505158.1:p.Asp918His
ENST00000679858.1:c.*2485G>C	ENSP00000505655.1:n.*2485G>C
ENST00000680211.1:c.-297G>C	ENSP00000506102.1:n.-297G>C
ENST00000680349.1:n.1086G>C
ENST00000680403.1:c.3103G>C	ENSP00000505677.1:p.Asp1035His
ENST00000680564.1:c.2972-703G>C	ENSP00000505582.1:n.2972-703G>C
ENST00000680590.1:c.*1498G>C	ENSP00000505350.1:n.*1498G>C
ENST00000680739.1:c.21G>C
ENST00000680773.1:n.1019G>C
ENST00000680806.1:c.*1821G>C	ENSP00000506418.1:n.*1821G>C
ENST00000680997.1:n.450G>C
ENST00000681088.1:c.765G>C
ENST00000681608.1:n.51G>C
ENST00000681625.1:c.*435G>C	ENSP00000505555.1:n.*435G>C
ENST00000270301.11:c.3103G>C	ENSP00000270301.6:p.Asp1035His
ENST00000401500.6:c.3103G>C	ENSP00000384792.1:p.Asp1035His
ENST00000587391.5:c.*2378G>C	ENSP00000465525.1:n.*2378G>C
NM_001083961.1:c.3103G>C	NP_001077430.1:p.Asp1035His
NM_173636.4:c.3103G>C	NP_775907.4:p.Asp1035His
XM_005258809.2:c.2992G>C	XP_005258866.1:p.Asp998His
XM_011526837.1:c.3088G>C	XP_011525139.1:p.Asp1030His
XM_011526838.1:c.2972-703G>C	XP_011525140.1:n.2972-703G>C
XM_011526839.1:c.2752G>C	XP_011525141.1:p.Asp918His
XM_011526840.1:c.2095G>C	XP_011525142.1:p.Asp699His
XM_011526841.1:c.1681G>C	XP_011525143.1:p.Asp561His
XM_011526842.1:c.1534G>C	XP_011525144.1:p.Asp512His
XM_011526843.1:c.850G>C	XP_011525145.1:p.Asp284His
XM_011526844.1:c.850G>C	XP_011525146.1:p.Asp284His
XM_011526840.2:c.2095G>C	XP_011525142.1:p.Asp699His
XM_011526841.2:c.1681G>C	XP_011525143.1:p.Asp561His
XM_011526844.2:c.850G>C	XP_011525146.1:p.Asp284His
XM_017026665.1:c.3103G>C	XP_016882154.1:p.Asp1035His
NM_001083961.2:c.3103G>C MANE Select	NP_001077430.1:p.Asp1035His
NM_173636.5:c.3103G>C	NP_775907.4:p.Asp1035His