Canonical Allele Identifier: CA357549157

Gene: WDFY3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.84733508G>C , CM000666.2:g.84733508G>C	GRCh38
NC_000004.11:g.85654661G>C , CM000666.1:g.85654661G>C	GRCh37
NC_000004.10:g.85873685G>C	NCBI36
NG_046917.1:g.237884C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014991.6:c.7095C>G MANE Select	NP_055806.2:p.His2365Gln
ENST00000295888.9:c.7095C>G MANE Select	ENSP00000295888.4:p.His2365Gln
NM_014991.4:c.7095C>G	NP_055806.2:p.His2365Gln
NM_014991.5:c.7095C>G	NP_055806.2:p.His2365Gln
ENST00000295888.8:c.7095C>G	ENSP00000295888.4:p.His2365Gln
ENST00000514711.2:c.5586C>G	ENSP00000424987.2:p.His1862Gln
XM_005262858.3:c.7149C>G	XP_005262915.1:p.His2383Gln
XM_005262858.5:c.7149C>G	XP_005262915.1:p.His2383Gln
XM_011531757.1:c.7149C>G	XP_011530059.1:p.His2383Gln
XM_011531757.3:c.7149C>G	XP_011530059.1:p.His2383Gln
XM_011531758.1:c.7149C>G	XP_011530060.1:p.His2383Gln
XM_011531759.1:c.7149C>G	XP_011530061.1:p.His2383Gln
XM_011531759.2:c.7149C>G	XP_011530061.1:p.His2383Gln
XM_011531760.1:c.7149C>G	XP_011530062.1:p.His2383Gln
XM_011531760.3:c.7149C>G	XP_011530062.1:p.His2383Gln
XM_011531761.1:c.7104C>G	XP_011530063.1:p.His2368Gln
XM_011531761.3:c.7104C>G	XP_011530063.1:p.His2368Gln
XM_011531762.1:c.7149C>G	XP_011530064.1:p.His2383Gln
XM_011531762.3:c.7149C>G	XP_011530064.1:p.His2383Gln
XM_011531763.1:c.7095C>G	XP_011530065.1:p.His2365Gln
XM_011531763.3:c.7095C>G	XP_011530065.1:p.His2365Gln
XM_011531764.1:c.7065C>G	XP_011530066.1:p.His2355Gln
XM_011531764.3:c.7065C>G	XP_011530066.1:p.His2355Gln
XM_011531765.1:c.7095C>G	XP_011530067.1:p.His2365Gln
XM_011531765.3:c.7095C>G	XP_011530067.1:p.His2365Gln
XM_017007906.2:c.7149C>G	XP_016863395.1:p.His2383Gln
XM_017007907.2:c.7149C>G	XP_016863396.1:p.His2383Gln
XM_017007908.2:c.7149C>G	XP_016863397.1:p.His2383Gln
XM_017007909.1:c.5115C>G	XP_016863398.1:p.His1705Gln