Canonical Allele Identifier: CA1324023420
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326231G= , CM000664.2:g.208326231G= GRCh38
NC_000002.11:g.209190955G= , CM000664.1:g.209190955G= GRCh37
NC_000002.10:g.208899200G= NCBI36
NG_021188.1:g.64965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3420G= MANE Select ENSP00000264380.4:p.Glu1140=
ENST00000264380.8:c.3420G= ENSP00000264380.4:p.Glu1140=
ENST00000452564.1:c.3252G= ENSP00000405736.1:p.Glu1084=
NM_015040.3:c.3420G= NP_055855.2:p.Glu1140=
XM_011510778.1:c.3456G= XP_011509080.1:p.Glu1152=
XM_011510779.1:c.3456G= XP_011509081.1:p.Glu1152=
XM_011510780.1:c.3453G= XP_011509082.1:p.Glu1151=
XM_011510781.1:c.3438G= XP_011509083.1:p.Glu1146=
XM_011510782.1:c.3456G= XP_011509084.1:p.Glu1152=
XM_011510783.1:c.3288G= XP_011509085.1:p.Glu1096=
XM_011510784.1:c.3285G= XP_011509086.1:p.Glu1095=
XM_011510785.1:c.3270G= XP_011509087.1:p.Glu1090=
XM_011510786.1:c.3165G= XP_011509088.1:p.Glu1055=
XM_011510787.1:c.3162G= XP_011509089.1:p.Glu1054=
XM_011510788.1:c.3129G= XP_011509090.1:p.Glu1043=
XM_011510789.1:c.2979G= XP_011509091.1:p.Glu993=
XM_011510790.1:c.2463G= XP_011509092.1:p.Glu821=
XM_011510791.1:c.2463G= XP_011509093.1:p.Glu821=
XM_011510792.1:c.3456G= XP_011509094.1:p.Glu1152=
XR_922888.1:n.3593G=
XM_011510778.3:c.3456G= XP_011509080.1:p.Glu1152=
XM_011510779.2:c.3456G= XP_011509081.1:p.Glu1152=
XM_011510780.2:c.3453G= XP_011509082.1:p.Glu1151=
XM_011510781.3:c.3438G= XP_011509083.1:p.Glu1146=
XM_011510782.3:c.3456G= XP_011509084.1:p.Glu1152=
XM_011510783.3:c.3288G= XP_011509085.1:p.Glu1096=
XM_011510784.2:c.3285G= XP_011509086.1:p.Glu1095=
XM_011510785.3:c.3270G= XP_011509087.1:p.Glu1090=
XM_011510786.3:c.3165G= XP_011509088.1:p.Glu1055=
XM_011510789.2:c.2979G= XP_011509091.1:p.Glu993=
XM_011510792.3:c.3456G= XP_011509094.1:p.Glu1152=
XM_017003568.1:c.3402G= XP_016859057.1:p.Glu1134=
XM_017003569.1:c.3234G= XP_016859058.1:p.Glu1078=
XM_017003570.1:c.2961G= XP_016859059.1:p.Glu987=
XM_017003571.1:c.2811G= XP_016859060.1:p.Glu937=
XM_017003572.1:c.2463G= XP_016859061.1:p.Glu821=
XM_017003573.1:c.2463G= XP_016859062.1:p.Glu821=
XM_017003574.1:c.2463G= XP_016859063.1:p.Glu821=
NM_015040.4:c.3420G= MANE Select NP_055855.2:p.Glu1140=