Canonical Allele Identifier: CA1324023480

Gene: PIKFYVE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208326366A= , CM000664.2:g.208326366A=	GRCh38
NC_000002.11:g.209191090A= , CM000664.1:g.209191090A=	GRCh37
NC_000002.10:g.208899335A=	NCBI36
NG_021188.1:g.65100A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264380.9:c.3555A= MANE Select	ENSP00000264380.4:p.Gly1185=
ENST00000264380.8:c.3555A=	ENSP00000264380.4:p.Gly1185=
ENST00000452564.1:c.3387A=	ENSP00000405736.1:p.Gly1129=
NM_015040.3:c.3555A=	NP_055855.2:p.Gly1185=
XM_011510778.1:c.3591A=	XP_011509080.1:p.Gly1197=
XM_011510779.1:c.3591A=	XP_011509081.1:p.Gly1197=
XM_011510780.1:c.3588A=	XP_011509082.1:p.Gly1196=
XM_011510781.1:c.3573A=	XP_011509083.1:p.Gly1191=
XM_011510782.1:c.3591A=	XP_011509084.1:p.Gly1197=
XM_011510783.1:c.3423A=	XP_011509085.1:p.Gly1141=
XM_011510784.1:c.3420A=	XP_011509086.1:p.Gly1140=
XM_011510785.1:c.3405A=	XP_011509087.1:p.Gly1135=
XM_011510786.1:c.3300A=	XP_011509088.1:p.Gly1100=
XM_011510787.1:c.3297A=	XP_011509089.1:p.Gly1099=
XM_011510788.1:c.3264A=	XP_011509090.1:p.Gly1088=
XM_011510789.1:c.3114A=	XP_011509091.1:p.Gly1038=
XM_011510790.1:c.2598A=	XP_011509092.1:p.Gly866=
XM_011510791.1:c.2598A=	XP_011509093.1:p.Gly866=
XM_011510792.1:c.3591A=	XP_011509094.1:p.Gly1197=
XR_922888.1:n.3728A=
XM_011510778.3:c.3591A=	XP_011509080.1:p.Gly1197=
XM_011510779.2:c.3591A=	XP_011509081.1:p.Gly1197=
XM_011510780.2:c.3588A=	XP_011509082.1:p.Gly1196=
XM_011510781.3:c.3573A=	XP_011509083.1:p.Gly1191=
XM_011510782.3:c.3591A=	XP_011509084.1:p.Gly1197=
XM_011510783.3:c.3423A=	XP_011509085.1:p.Gly1141=
XM_011510784.2:c.3420A=	XP_011509086.1:p.Gly1140=
XM_011510785.3:c.3405A=	XP_011509087.1:p.Gly1135=
XM_011510786.3:c.3300A=	XP_011509088.1:p.Gly1100=
XM_011510789.2:c.3114A=	XP_011509091.1:p.Gly1038=
XM_011510792.3:c.3591A=	XP_011509094.1:p.Gly1197=
XM_017003568.1:c.3537A=	XP_016859057.1:p.Gly1179=
XM_017003569.1:c.3369A=	XP_016859058.1:p.Gly1123=
XM_017003570.1:c.3096A=	XP_016859059.1:p.Gly1032=
XM_017003571.1:c.2946A=	XP_016859060.1:p.Gly982=
XM_017003572.1:c.2598A=	XP_016859061.1:p.Gly866=
XM_017003573.1:c.2598A=	XP_016859062.1:p.Gly866=
XM_017003574.1:c.2598A=	XP_016859063.1:p.Gly866=
NM_015040.4:c.3555A= MANE Select	NP_055855.2:p.Gly1185=