Canonical Allele Identifier: CA1324023461
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326326A= , CM000664.2:g.208326326A= GRCh38
NC_000002.11:g.209191050A= , CM000664.1:g.209191050A= GRCh37
NC_000002.10:g.208899295A= NCBI36
NG_021188.1:g.65060A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3515A= MANE Select ENSP00000264380.4:p.His1172=
ENST00000264380.8:c.3515A= ENSP00000264380.4:p.His1172=
ENST00000452564.1:c.3347A= ENSP00000405736.1:p.His1116=
NM_015040.3:c.3515A= NP_055855.2:p.His1172=
XM_011510778.1:c.3551A= XP_011509080.1:p.His1184=
XM_011510779.1:c.3551A= XP_011509081.1:p.His1184=
XM_011510780.1:c.3548A= XP_011509082.1:p.His1183=
XM_011510781.1:c.3533A= XP_011509083.1:p.His1178=
XM_011510782.1:c.3551A= XP_011509084.1:p.His1184=
XM_011510783.1:c.3383A= XP_011509085.1:p.His1128=
XM_011510784.1:c.3380A= XP_011509086.1:p.His1127=
XM_011510785.1:c.3365A= XP_011509087.1:p.His1122=
XM_011510786.1:c.3260A= XP_011509088.1:p.His1087=
XM_011510787.1:c.3257A= XP_011509089.1:p.His1086=
XM_011510788.1:c.3224A= XP_011509090.1:p.His1075=
XM_011510789.1:c.3074A= XP_011509091.1:p.His1025=
XM_011510790.1:c.2558A= XP_011509092.1:p.His853=
XM_011510791.1:c.2558A= XP_011509093.1:p.His853=
XM_011510792.1:c.3551A= XP_011509094.1:p.His1184=
XR_922888.1:n.3688A=
XM_011510778.3:c.3551A= XP_011509080.1:p.His1184=
XM_011510779.2:c.3551A= XP_011509081.1:p.His1184=
XM_011510780.2:c.3548A= XP_011509082.1:p.His1183=
XM_011510781.3:c.3533A= XP_011509083.1:p.His1178=
XM_011510782.3:c.3551A= XP_011509084.1:p.His1184=
XM_011510783.3:c.3383A= XP_011509085.1:p.His1128=
XM_011510784.2:c.3380A= XP_011509086.1:p.His1127=
XM_011510785.3:c.3365A= XP_011509087.1:p.His1122=
XM_011510786.3:c.3260A= XP_011509088.1:p.His1087=
XM_011510789.2:c.3074A= XP_011509091.1:p.His1025=
XM_011510792.3:c.3551A= XP_011509094.1:p.His1184=
XM_017003568.1:c.3497A= XP_016859057.1:p.His1166=
XM_017003569.1:c.3329A= XP_016859058.1:p.His1110=
XM_017003570.1:c.3056A= XP_016859059.1:p.His1019=
XM_017003571.1:c.2906A= XP_016859060.1:p.His969=
XM_017003572.1:c.2558A= XP_016859061.1:p.His853=
XM_017003573.1:c.2558A= XP_016859062.1:p.His853=
XM_017003574.1:c.2558A= XP_016859063.1:p.His853=
NM_015040.4:c.3515A= MANE Select NP_055855.2:p.His1172=