Canonical Allele Identifier: CA100717829

Gene: WDFY3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.84682443G>A , CM000666.2:g.84682443G>A	GRCh38
NC_000004.11:g.85603596G>A , CM000666.1:g.85603596G>A	GRCh37
NC_000004.10:g.85822620G>A	NCBI36
NG_046917.1:g.288949C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014991.6:c.9754C>T MANE Select	NP_055806.2:p.Pro3252Ser
ENST00000295888.9:c.9754C>T MANE Select	ENSP00000295888.4:p.Pro3252Ser
NM_014991.4:c.9754C>T	NP_055806.2:p.Pro3252Ser
NM_014991.5:c.9754C>T	NP_055806.2:p.Pro3252Ser
ENST00000295888.8:c.9754C>T	ENSP00000295888.4:p.Pro3252Ser
ENST00000425179.2:n.506C>T
ENST00000514711.2:c.8194C>T	ENSP00000424987.2:p.Pro2732Ser
XM_005262858.3:c.9808C>T	XP_005262915.1:p.Pro3270Ser
XM_005262858.5:c.9808C>T	XP_005262915.1:p.Pro3270Ser
XM_011531757.1:c.9808C>T	XP_011530059.1:p.Pro3270Ser
XM_011531757.3:c.9808C>T	XP_011530059.1:p.Pro3270Ser
XM_011531758.1:c.9808C>T	XP_011530060.1:p.Pro3270Ser
XM_011531759.1:c.9808C>T	XP_011530061.1:p.Pro3270Ser
XM_011531759.2:c.9808C>T	XP_011530061.1:p.Pro3270Ser
XM_011531760.1:c.9808C>T	XP_011530062.1:p.Pro3270Ser
XM_011531760.3:c.9808C>T	XP_011530062.1:p.Pro3270Ser
XM_011531761.1:c.9763C>T	XP_011530063.1:p.Pro3255Ser
XM_011531761.3:c.9763C>T	XP_011530063.1:p.Pro3255Ser
XM_011531762.1:c.9757C>T	XP_011530064.1:p.Pro3253Ser
XM_011531762.3:c.9757C>T	XP_011530064.1:p.Pro3253Ser
XM_011531763.1:c.9754C>T	XP_011530065.1:p.Pro3252Ser
XM_011531763.3:c.9754C>T	XP_011530065.1:p.Pro3252Ser
XM_011531764.1:c.9724C>T	XP_011530066.1:p.Pro3242Ser
XM_011531764.3:c.9724C>T	XP_011530066.1:p.Pro3242Ser
XM_011531765.1:c.9703C>T	XP_011530067.1:p.Pro3235Ser
XM_011531765.3:c.9703C>T	XP_011530067.1:p.Pro3235Ser
XM_017007906.2:c.9808C>T	XP_016863395.1:p.Pro3270Ser
XM_017007907.2:c.9808C>T	XP_016863396.1:p.Pro3270Ser
XM_017007908.2:c.9808C>T	XP_016863397.1:p.Pro3270Ser
XM_017007909.1:c.7774C>T	XP_016863398.1:p.Pro2592Ser