Canonical Allele Identifier: CA1908424038

Gene: WDFY4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48817351G= , CM000672.2:g.48817351G=	GRCh38
NC_000010.10:g.50025396G= , CM000672.1:g.50025396G=	GRCh37
NC_000010.9:g.49695402G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325239.12:c.5447G= MANE Select	ENSP00000320563.5:p.Arg1816=
ENST00000325239.11:c.5447G=	ENSP00000320563.5:p.Arg1816=
ENST00000325239.9:c.5447G=	ENSP00000320563.5:p.Arg1816=
ENST00000374161.7:c.1086G=
NM_020945.1:c.5447G=	NP_065996.1:p.Arg1816=
XM_005270004.2:c.5447G=	XP_005270061.1:p.Arg1816=
XM_011539986.1:c.5447G=	XP_011538288.1:p.Arg1816=
XM_011539987.1:c.5447G=	XP_011538289.1:p.Arg1816=
XM_011539988.1:c.5447G=	XP_011538290.1:p.Arg1816=
XM_011539989.1:c.5567G=	XP_011538291.1:p.Arg1856=
XM_011539990.1:c.5567G=	XP_011538292.1:p.Arg1856=
XM_011539991.1:c.5567G=	XP_011538293.1:p.Arg1856=
XM_005270004.3:c.5447G=	XP_005270061.1:p.Arg1816=
XM_011539986.3:c.5567G=	XP_011538288.2:p.Arg1856=
XM_011539987.2:c.5567G=	XP_011538289.2:p.Arg1856=
XM_011539988.2:c.5447G=	XP_011538290.1:p.Arg1816=
XM_011539990.3:c.5567G=	XP_011538292.1:p.Arg1856=
XM_011539991.3:c.5567G=	XP_011538293.1:p.Arg1856=
XM_017016463.1:c.5447G=	XP_016871952.1:p.Arg1816=
XM_017016464.1:c.1871G=	XP_016871953.1:p.Arg624=
NM_020945.2:c.5447G=	NP_065996.1:p.Arg1816=
NM_001394531.1:c.5447G= MANE Select	NP_001381460.1:p.Arg1816=