Canonical Allele Identifier: CA1324023427
Gene: PIKFYVE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208326242A= , CM000664.2:g.208326242A= GRCh38
NC_000002.11:g.209190966A= , CM000664.1:g.209190966A= GRCh37
NC_000002.10:g.208899211A= NCBI36
NG_021188.1:g.64976A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264380.9:c.3431A= MANE Select ENSP00000264380.4:p.Asp1144=
ENST00000264380.8:c.3431A= ENSP00000264380.4:p.Asp1144=
ENST00000452564.1:c.3263A= ENSP00000405736.1:p.Asp1088=
NM_015040.3:c.3431A= NP_055855.2:p.Asp1144=
XM_011510778.1:c.3467A= XP_011509080.1:p.Asp1156=
XM_011510779.1:c.3467A= XP_011509081.1:p.Asp1156=
XM_011510780.1:c.3464A= XP_011509082.1:p.Asp1155=
XM_011510781.1:c.3449A= XP_011509083.1:p.Asp1150=
XM_011510782.1:c.3467A= XP_011509084.1:p.Asp1156=
XM_011510783.1:c.3299A= XP_011509085.1:p.Asp1100=
XM_011510784.1:c.3296A= XP_011509086.1:p.Asp1099=
XM_011510785.1:c.3281A= XP_011509087.1:p.Asp1094=
XM_011510786.1:c.3176A= XP_011509088.1:p.Asp1059=
XM_011510787.1:c.3173A= XP_011509089.1:p.Asp1058=
XM_011510788.1:c.3140A= XP_011509090.1:p.Asp1047=
XM_011510789.1:c.2990A= XP_011509091.1:p.Asp997=
XM_011510790.1:c.2474A= XP_011509092.1:p.Asp825=
XM_011510791.1:c.2474A= XP_011509093.1:p.Asp825=
XM_011510792.1:c.3467A= XP_011509094.1:p.Asp1156=
XR_922888.1:n.3604A=
XM_011510778.3:c.3467A= XP_011509080.1:p.Asp1156=
XM_011510779.2:c.3467A= XP_011509081.1:p.Asp1156=
XM_011510780.2:c.3464A= XP_011509082.1:p.Asp1155=
XM_011510781.3:c.3449A= XP_011509083.1:p.Asp1150=
XM_011510782.3:c.3467A= XP_011509084.1:p.Asp1156=
XM_011510783.3:c.3299A= XP_011509085.1:p.Asp1100=
XM_011510784.2:c.3296A= XP_011509086.1:p.Asp1099=
XM_011510785.3:c.3281A= XP_011509087.1:p.Asp1094=
XM_011510786.3:c.3176A= XP_011509088.1:p.Asp1059=
XM_011510789.2:c.2990A= XP_011509091.1:p.Asp997=
XM_011510792.3:c.3467A= XP_011509094.1:p.Asp1156=
XM_017003568.1:c.3413A= XP_016859057.1:p.Asp1138=
XM_017003569.1:c.3245A= XP_016859058.1:p.Asp1082=
XM_017003570.1:c.2972A= XP_016859059.1:p.Asp991=
XM_017003571.1:c.2822A= XP_016859060.1:p.Asp941=
XM_017003572.1:c.2474A= XP_016859061.1:p.Asp825=
XM_017003573.1:c.2474A= XP_016859062.1:p.Asp825=
XM_017003574.1:c.2474A= XP_016859063.1:p.Asp825=
NM_015040.4:c.3431A= MANE Select NP_055855.2:p.Asp1144=