Canonical Allele Identifier: CA2992259

Gene: WDFY3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.84691741T>C , CM000666.2:g.84691741T>C	GRCh38
NC_000004.11:g.85612894T>C , CM000666.1:g.85612894T>C	GRCh37
NC_000004.10:g.85831918T>C	NCBI36
NG_046917.1:g.279651A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014991.6:c.9094A>G MANE Select	NP_055806.2:p.Ile3032Val
ENST00000295888.9:c.9094A>G MANE Select	ENSP00000295888.4:p.Ile3032Val
NM_014991.4:c.9094A>G	NP_055806.2:p.Ile3032Val
NM_014991.5:c.9094A>G	NP_055806.2:p.Ile3032Val
ENST00000295888.8:c.9094A>G	ENSP00000295888.4:p.Ile3032Val
ENST00000514711.1:c.1903A>G	ENSP00000424987.1:p.Ile635Val
ENST00000514711.2:c.7534A>G	ENSP00000424987.2:p.Ile2512Val
XM_005262858.3:c.9148A>G	XP_005262915.1:p.Ile3050Val
XM_005262858.5:c.9148A>G	XP_005262915.1:p.Ile3050Val
XM_011531757.1:c.9148A>G	XP_011530059.1:p.Ile3050Val
XM_011531757.3:c.9148A>G	XP_011530059.1:p.Ile3050Val
XM_011531758.1:c.9148A>G	XP_011530060.1:p.Ile3050Val
XM_011531759.1:c.9148A>G	XP_011530061.1:p.Ile3050Val
XM_011531759.2:c.9148A>G	XP_011530061.1:p.Ile3050Val
XM_011531760.1:c.9148A>G	XP_011530062.1:p.Ile3050Val
XM_011531760.3:c.9148A>G	XP_011530062.1:p.Ile3050Val
XM_011531761.1:c.9103A>G	XP_011530063.1:p.Ile3035Val
XM_011531761.3:c.9103A>G	XP_011530063.1:p.Ile3035Val
XM_011531762.1:c.9097A>G	XP_011530064.1:p.Ile3033Val
XM_011531762.3:c.9097A>G	XP_011530064.1:p.Ile3033Val
XM_011531763.1:c.9094A>G	XP_011530065.1:p.Ile3032Val
XM_011531763.3:c.9094A>G	XP_011530065.1:p.Ile3032Val
XM_011531764.1:c.9064A>G	XP_011530066.1:p.Ile3022Val
XM_011531764.3:c.9064A>G	XP_011530066.1:p.Ile3022Val
XM_011531765.1:c.9043A>G	XP_011530067.1:p.Ile3015Val
XM_011531765.3:c.9043A>G	XP_011530067.1:p.Ile3015Val
XM_017007906.2:c.9148A>G	XP_016863395.1:p.Ile3050Val
XM_017007907.2:c.9148A>G	XP_016863396.1:p.Ile3050Val
XM_017007908.2:c.9148A>G	XP_016863397.1:p.Ile3050Val
XM_017007909.1:c.7114A>G	XP_016863398.1:p.Ile2372Val