Canonical Allele Identifier: CA405426316

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36556882T>G (hg19) ; chr19:g.36065980T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36065980T>G , CM000681.2:g.36065980T>G	GRCh38
NC_000019.9:g.36556882T>G , CM000681.1:g.36556882T>G	GRCh37
NC_000019.8:g.41248722T>G	NCBI36
NG_028101.1:g.16100T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.355T>G	ENSP00000270301.6:p.Phe119Val
ENST00000401500.7:c.355T>G MANE Select	ENSP00000384792.1:p.Phe119Val
ENST00000427823.3:c.439T>G	ENSP00000413475.4:p.Phe147Val
ENST00000587391.6:c.355T>G	ENSP00000465525.1:p.Phe119Val
ENST00000589953.2:n.419T>G
ENST00000644764.2:c.355T>G	ENSP00000494253.2:p.Phe119Val
ENST00000679682.1:c.355T>G	ENSP00000506226.1:p.Phe119Val
ENST00000679714.1:c.355T>G	ENSP00000506627.1:p.Phe119Val
ENST00000679757.1:c.355T>G	ENSP00000505158.1:p.Phe119Val
ENST00000679858.1:c.355T>G	ENSP00000505655.1:p.Phe119Val
ENST00000680321.1:c.355T>G	ENSP00000505525.1:p.Phe119Val
ENST00000680359.1:c.355T>G	ENSP00000506079.1:p.Phe119Val
ENST00000680403.1:c.355T>G	ENSP00000505677.1:p.Phe119Val
ENST00000680489.1:n.678T>G
ENST00000680564.1:c.355T>G	ENSP00000505582.1:p.Phe119Val
ENST00000680590.1:c.355T>G	ENSP00000505350.1:p.Phe119Val
ENST00000680806.1:c.355T>G	ENSP00000506418.1:p.Phe119Val
ENST00000681542.1:c.355T>G	ENSP00000505251.1:p.Phe119Val
ENST00000681625.1:c.355T>G	ENSP00000505555.1:p.Phe119Val
ENST00000681809.1:c.355T>G	ENSP00000505740.1:p.Phe119Val
ENST00000270301.11:c.355T>G	ENSP00000270301.6:p.Phe119Val
ENST00000378860.8:n.446T>G
ENST00000401500.6:c.355T>G	ENSP00000384792.1:p.Phe119Val
ENST00000427823.2:c.421T>G	ENSP00000413475.3:p.Phe141Val
ENST00000587391.5:c.355T>G	ENSP00000465525.1:p.Phe119Val
NM_001083961.1:c.355T>G	NP_001077430.1:p.Phe119Val
NM_173636.4:c.355T>G	NP_775907.4:p.Phe119Val
XM_005258809.2:c.355T>G	XP_005258866.1:p.Phe119Val
XM_011526837.1:c.355T>G	XP_011525139.1:p.Phe119Val
XM_011526838.1:c.355T>G	XP_011525140.1:p.Phe119Val
XM_011526839.1:c.355T>G	XP_011525141.1:p.Phe119Val
XM_017026665.1:c.355T>G	XP_016882154.1:p.Phe119Val
XR_001753671.1:n.446T>G
XR_001753672.1:n.446T>G
NM_001083961.2:c.355T>G MANE Select	NP_001077430.1:p.Phe119Val
NM_173636.5:c.355T>G	NP_775907.4:p.Phe119Val