Canonical Allele Identifier: CA357541222

Gene: WDFY3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.84715349C>T , CM000666.2:g.84715349C>T	GRCh38
NC_000004.11:g.85636502C>T , CM000666.1:g.85636502C>T	GRCh37
NC_000004.10:g.85855526C>T	NCBI36
NG_046917.1:g.256043G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014991.6:c.7910G>A MANE Select	NP_055806.2:p.Arg2637Gln
ENST00000295888.9:c.7910G>A MANE Select	ENSP00000295888.4:p.Arg2637Gln
NM_014991.4:c.7910G>A	NP_055806.2:p.Arg2637Gln
NM_014991.5:c.7910G>A	NP_055806.2:p.Arg2637Gln
ENST00000295888.8:c.7910G>A	ENSP00000295888.4:p.Arg2637Gln
ENST00000514711.1:c.719G>A	ENSP00000424987.1:p.Arg240Gln
ENST00000514711.2:c.6350G>A	ENSP00000424987.2:p.Arg2117Gln
XM_005262858.3:c.7964G>A	XP_005262915.1:p.Arg2655Gln
XM_005262858.5:c.7964G>A	XP_005262915.1:p.Arg2655Gln
XM_011531757.1:c.7964G>A	XP_011530059.1:p.Arg2655Gln
XM_011531757.3:c.7964G>A	XP_011530059.1:p.Arg2655Gln
XM_011531758.1:c.7964G>A	XP_011530060.1:p.Arg2655Gln
XM_011531759.1:c.7964G>A	XP_011530061.1:p.Arg2655Gln
XM_011531759.2:c.7964G>A	XP_011530061.1:p.Arg2655Gln
XM_011531760.1:c.7964G>A	XP_011530062.1:p.Arg2655Gln
XM_011531760.3:c.7964G>A	XP_011530062.1:p.Arg2655Gln
XM_011531761.1:c.7919G>A	XP_011530063.1:p.Arg2640Gln
XM_011531761.3:c.7919G>A	XP_011530063.1:p.Arg2640Gln
XM_011531762.1:c.7913G>A	XP_011530064.1:p.Arg2638Gln
XM_011531762.3:c.7913G>A	XP_011530064.1:p.Arg2638Gln
XM_011531763.1:c.7910G>A	XP_011530065.1:p.Arg2637Gln
XM_011531763.3:c.7910G>A	XP_011530065.1:p.Arg2637Gln
XM_011531764.1:c.7880G>A	XP_011530066.1:p.Arg2627Gln
XM_011531764.3:c.7880G>A	XP_011530066.1:p.Arg2627Gln
XM_011531765.1:c.7859G>A	XP_011530067.1:p.Arg2620Gln
XM_011531765.3:c.7859G>A	XP_011530067.1:p.Arg2620Gln
XM_017007906.2:c.7964G>A	XP_016863395.1:p.Arg2655Gln
XM_017007907.2:c.7964G>A	XP_016863396.1:p.Arg2655Gln
XM_017007908.2:c.7964G>A	XP_016863397.1:p.Arg2655Gln
XM_017007909.1:c.5930G>A	XP_016863398.1:p.Arg1977Gln