Canonical Allele Identifier: CA405449947

Gene: WDR62

Linked Data

• dbSNP Id: rs1279249772
• gnomAD v2: 19-36592928-C-G
• gnomAD v4: 19-36102026-C-G
• MyVariant Identifiers: chr19:g.36592928C>G (hg19) ; chr19:g.36102026C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102026C>G , CM000681.2:g.36102026C>G	GRCh38
NC_000019.9:g.36592928C>G , CM000681.1:g.36592928C>G	GRCh37
NC_000019.8:g.41284768C>G	NCBI36
NG_028101.1:g.52146C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3095C>G	ENSP00000270301.6:p.Pro1032Arg
ENST00000401500.7:c.3095C>G MANE Select	ENSP00000384792.1:p.Pro1032Arg
ENST00000587391.6:c.*2370C>G	ENSP00000465525.1:n.*2370C>G
ENST00000679357.1:c.885C>G
ENST00000679422.1:c.774C>G
ENST00000679682.1:c.3080C>G	ENSP00000506226.1:p.Pro1027Arg
ENST00000679714.1:c.3089C>G	ENSP00000506627.1:p.Pro1030Arg
ENST00000679757.1:c.2744C>G	ENSP00000505158.1:p.Pro915Arg
ENST00000679858.1:c.*2477C>G	ENSP00000505655.1:n.*2477C>G
ENST00000680211.1:c.-305C>G	ENSP00000506102.1:n.-305C>G
ENST00000680349.1:n.1078C>G
ENST00000680403.1:c.3095C>G	ENSP00000505677.1:p.Pro1032Arg
ENST00000680564.1:c.2971+709C>G	ENSP00000505582.1:n.2971+709C>G
ENST00000680590.1:c.*1490C>G	ENSP00000505350.1:n.*1490C>G
ENST00000680739.1:c.13C>G
ENST00000680773.1:n.1011C>G
ENST00000680806.1:c.*1813C>G	ENSP00000506418.1:n.*1813C>G
ENST00000680997.1:n.442C>G
ENST00000681088.1:c.757C>G
ENST00000681608.1:n.43C>G
ENST00000681625.1:c.*427C>G	ENSP00000505555.1:n.*427C>G
ENST00000270301.11:c.3095C>G	ENSP00000270301.6:p.Pro1032Arg
ENST00000401500.6:c.3095C>G	ENSP00000384792.1:p.Pro1032Arg
ENST00000587391.5:c.*2370C>G	ENSP00000465525.1:n.*2370C>G
NM_001083961.1:c.3095C>G	NP_001077430.1:p.Pro1032Arg
NM_173636.4:c.3095C>G	NP_775907.4:p.Pro1032Arg
XM_005258809.2:c.2984C>G	XP_005258866.1:p.Pro995Arg
XM_011526837.1:c.3080C>G	XP_011525139.1:p.Pro1027Arg
XM_011526838.1:c.2971+709C>G	XP_011525140.1:n.2971+709C>G
XM_011526839.1:c.2744C>G	XP_011525141.1:p.Pro915Arg
XM_011526840.1:c.2087C>G	XP_011525142.1:p.Pro696Arg
XM_011526841.1:c.1673C>G	XP_011525143.1:p.Pro558Arg
XM_011526842.1:c.1526C>G	XP_011525144.1:p.Pro509Arg
XM_011526843.1:c.842C>G	XP_011525145.1:p.Pro281Arg
XM_011526844.1:c.842C>G	XP_011525146.1:p.Pro281Arg
XM_011526840.2:c.2087C>G	XP_011525142.1:p.Pro696Arg
XM_011526841.2:c.1673C>G	XP_011525143.1:p.Pro558Arg
XM_011526844.2:c.842C>G	XP_011525146.1:p.Pro281Arg
XM_017026665.1:c.3095C>G	XP_016882154.1:p.Pro1032Arg
NM_001083961.2:c.3095C>G MANE Select	NP_001077430.1:p.Pro1032Arg
NM_173636.5:c.3095C>G	NP_775907.4:p.Pro1032Arg